HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242972Generated: October 26, 2026
Triethylamine → [(S)-1-(3-Phenylaminopyridin-2-ylcarbamoyl)ethyl]carbamic acid tert-butyl ester
https://huagongshe.com/reaction/242972
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Tert-butoxycarbonylalanine | HCID 85082 | — |
| Reactant | HOAt | HCID 181649 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | N3-Phenylpyridine-2,3-diamine | HCID 68018423 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | [(S)-1-(3-Phenylaminopyridin-2-ylcarbamoyl)ethyl]carbamic acid tert-butyl ester | HCID 68156995 | 119.4% |
Reaction Steps
Triethylamine (1.5 mL, 11.0 mmol) was added to a mixture of N3-phenylpyridine-2,3-diamine (510 mg, 2.75 mmol), (S)-2-tertbutoxycarbonylaminopropionic acid (0.94 g, 4.96 mmol), HOAt (670 mg, 4.96 mmol) and N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (0.95 g, 4.96 mmol) in anhydrous DCM (30 mL) at 0° C. under a nitrogen atmosphere. The reaction mixture was stirred at 0° C. for 10 min then slowly warmed to RT. Stirring at RT was continued for 18 h. The reaction mixture was partitioned between DCM and a saturated aqueous solution of NaHCO3. The aqueous phase was further extracted with DCM (×3) and the combined organic fractions washed with water, dried (Na2SO4) and concentrated in vacuo to afford the title compound as a light brown foam (1.17 g, quantitative). LCMS (Method C): RT 3.04 min [M+H]+ 357.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08653089B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-6dcae8cfbd1d486e830b3fd87d3e6bd1 |
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| Source note | uspto-grants-2014_02 |
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