Eli Lilly · Boulder, Colorado
David N. Primer, Ph.D.
Director, CMC Process Chemistry
Senior process chemistry leader translating discovery-stage oncology programs into scalable, GMP-ready manufacturing routes.
About
Process chemistry, end to end.
I lead CMC process chemistry teams that develop, optimize, and scale the synthetic routes behind oncology drug candidates — moving programs from gram-scale discovery deliveries through hundred-kilogram GMP manufacture.
My work sits at the intersection of synthetic invention, crystallization and form control, vendor and tech-transfer management, and the practical realities of clinical-supply timelines. Earlier in my career I co-developed the photoredox / nickel dual-catalysis cross-coupling strategy that opened up C(sp2)–C(sp3) bond formation as a routine pharmaceutical disconnection.
- Peer-reviewed publications
- 15
- Patents
- 3
- Largest GMP scale led
- >400 kg
- Direct reports mentored
- 8
Education
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University of Pennsylvania
2012 – 2017
Ph.D., Organic Chemistry
GPA 3.97 / 4.00 · Advisor: Prof. Gary A. Molander · Thesis: Single-Electron Transmetalation: Radical-Mediated Alkyl Transfer in Cross-Coupling.
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Emory University
2008 – 2012
B.S., Chemistry
GPA 3.37 / 4.00 · Undergraduate research with Prof. Huw M. L. Davies on chiral silver and gold carbenoid reactivity.
Industry experience
Selected roles
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Eli Lilly
Director, CMC Process Chemistry
2022 – present
Boulder, CO
- Lead and develop the CMC process chemistry team — coordinating project assignments, technical training, and career development.
- CMC project lead for LSN4170130, coordinating across three external vendors, discovery partners, and the broader CMC development team.
- Developed the 4-step GMP route for LY4050784, internally delivering 500 g for GLP tox on an accelerated timeline; the process has since scaled to >100 kg at multiple GMP vendors.
- Developed the 5-step GMP route for LY3866288 and led tech transfer activities that cut timelines by 70% and costs by 50% — keeping Phase 1 plans on pace for accelerated approval; scaled to >400 kg externally.
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Bristol Myers Squibb
Senior Scientist / Principal Scientist, Chemical Process Development
2020 – 2022
New Brunswick, NJ
- Optimized the final three steps of the CC-94676 (BMS-986365) synthesis — delivering >12 kg of Phase 1 material as racemate and as both single diastereomers in high chemical and enantiomeric purity.
- Managed and trained two scientists on process development and route scouting toward a key intermediate in the bifunctional degrader portfolio.
- Identified multiple crystalline forms of a high-MW (>900) greasy API, enabling the program to transition from amorphous precipitation to a controlled crystallization.
- Provided technical leadership for tech transfers to partner sites in Colorado, Wisconsin, India, and China.
- Co-designed browser-based high-throughput-experimentation software with ACD Labs and internal IT, improving data capture across the solubility, catalysis, and class-variable screening groups.
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Celgene Corporation
Scientist I / II, Drug Substance Development
2017 – 2020
Summit, NJ
- Developed a crystallization-induced resolution of a racemic amine — providing the first commercial-scale access to the single-enantiomer of a glutarimide-containing scaffold.
- Scaled three processes from 500 g to >20 kg, supporting on-site manufacturing in Switzerland, the United Kingdom, and the United States for the synthesis of Iberdomide.
- Filed a patent application and published a peer-reviewed paper on the novel processes developed for CC-90010.
Selected publications
Peer-reviewed work.
Fourteen peer-reviewed publications and two issued patents, with co-authorship in Nature, Science, JACS, Nature Protocols, and OPRD. Click any cover to read the article.
Citation counts and the full bibliography are tracked on Google Scholar.
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Highlight
Nature · 2024
Identifying General Reaction Conditions by Bandit Optimization
J. Y. Wang, J. M. Stevens, S. K. Kariofillis, M. Tom, D. L. Golden, J. Li, J. E. Tabora, M. Parasram, B. J. Shields, D. N. Primer, B. Hao, D. Del Valle, S. DiSomma, A. Furman, G. G. Zipp, S. Melnikov, J. Paulson, A. G. Doyle
626, 1025–1033
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Highlight
Journal of the American Chemical Society · 2017
Enabling the Cross-Coupling of Tertiary Organoboron Nucleophiles through Radical-Mediated Alkyl Transfer
D. N. Primer, G. A. Molander
139, 9847–9850
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Highlight
Science · 2014
Single-Electron Transmetalation in Organoboron Cross-Coupling by Photoredox/Nickel Dual Catalysis
J. C. Tellis, D. N. Primer, G. A. Molander
345, 433–436 · Co-first author
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Organic Process Research & Development · 2024
Process Development and Kilogram-Scale Manufacture of Key Intermediates toward Single-Enantiomer CELMoDs: Synthesis of Iberdomide·BSA, Part 1
M. J. Zacuto, J. F. Traverse, K. F. Bostwick, M. E. Geherty, D. N. Primer, W. Zhang, C. Zhang, R. D. Janes, C. Marton
28, 46–56
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Organic Process Research & Development · 2022
Development of a Process to a 4-Arylated 2-Methylisoquinolin-1(2H)-one for the Treatment of Solid Tumors: Lessons in Ortho-Bromination, Selective Solubility, Pd Deactivation, and Form Control
D. N. Primer, K. Yong, A. Ramirez, M. Kreilein, A. C. Ferretti, A. M. Ruda, N. Fleary-Roberts, J. D. Moseley, S. M. Forsyth, G. R. Evans, J. F. Traverse
26, 1458–1469
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Nature Protocols · 2017
Preparation of Visible-Light-Activated Metal Complexes and Their Use in Photoredox/Nickel Dual Catalysis
C. B. Kelly, N. R. Patel, D. N. Primer, M. Jouffroy, J. C. Tellis, G. A. Molander
12, 472–492
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Chemical Science · 2017
Metal-Free C–H Alkylation of Heteroarenes with Alkyltrifluoroborates
J. K. Matsui, D. N. Primer, G. A. Molander
8, 3512–3522
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ACS Catalysis · 2017
Nickel/Photoredox-Catalyzed Amidation via Alkylsilicates and Isocyanates
S. Zheng, D. N. Primer, G. A. Molander
7, 7957–7961
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Accounts of Chemical Research · 2016
Single-Electron Transmetalation via Photoredox/Nickel Dual Catalysis
J. C. Tellis, C. B. Kelly, D. N. Primer, M. Jouffroy, N. R. Patel, G. A. Molander
49, 1429–1439
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Journal of the American Chemical Society · 2016
Base-Free Photoredox/Nickel Dual-Catalytic Cross-Coupling of Ammonium Alkylsilicates
M. Jouffroy, D. N. Primer, G. A. Molander
138, 475–478
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Chemistry – A European Journal · 2016
Single-Electron Transmetalation: Synthesis of 1,1-Diaryl-2,2,2-trifluoroethanes by Photoredox/Nickel Dual Catalysis
D. W. Ryu, D. N. Primer, J. C. Tellis, G. A. Molander
22, 120–123
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Journal of the American Chemical Society · 2015
Nickel-Catalyzed Cross-Coupling of Photoredox-Generated Radicals: Uncovering a General Manifold for Stereoconvergence
O. Gutierrez, J. C. Tellis, D. N. Primer, G. A. Molander, M. C. Kozlowski
137, 4896–4899
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Journal of the American Chemical Society · 2015
Single-Electron Transmetalation: An Enabling Technology for Secondary Alkylboron Cross-Coupling
D. N. Primer, I. Karakaya, J. C. Tellis, G. A. Molander
137, 2195–2198
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Organic Letters · 2015
Photoredox Cross-Coupling: Ir/Ni Dual Catalysis for the Synthesis of Benzylic Ethers
I. Karakaya, D. N. Primer, G. A. Molander
17, 3294–3297
Patents
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US Patent Application · 2025
Processes for the Preparation of Substituted 3-((3-Aminophenyl)amino)piperidine-2,6-dione Compounds
G. Beutner, R. Carrasquillo, W. P. Gallagher, M. Geherty, J. Han, K. Jones, et al.
19/201,806
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US Patent · 2023
Process for the Preparation of a Bromodomain Inhibitor
J. F. Traverse, K. H. Y. Yong, A. C. Ferretti, H. Alite, J. Moseley, A. M. Ruda, et al.
11,566,004
A third patent application is pending and will be added once published.
Recognition
- ACS Organic Division Early Career Investigator Award — winner Aug 2026
- Heterocycles Gordon Conference — Invited 45-min talk on CC-90010 synthesis and scale-up Jun 2022
- UPenn Dissertation Completion Fellowship — 9-month award for outstanding research 2016 – 2017
- IPMI Sabin Metal Corp. Student Award — $5,000 for outstanding precious-metals research Jun 2016
- Genentech Graduate Student Symposium — $1,000 honorarium for oral presentation May 2016
- NIH grant GM-113878 — co-author; funded the lab for four years 2015
Contact
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