HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 243139Generated: October 29, 2026
Tert-butoxycarbonylalanine → [(S)-1-(3-Bromo-2-cyclopropylamino-4-fluorophenylcarbamoyl)ethyl]carbamic acid tert-butyl ester
https://huagongshe.com/reaction/243139
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tert-butoxycarbonylalanine | HCID 85082 | — |
| Reactant | HOAt | HCID 181649 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 3-Bromo-N2-cyclopropyl-4-fluorobenzene-1,2-diamine | HCID 68157591 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | [(S)-1-(3-Bromo-2-cyclopropylamino-4-fluorophenylcarbamoyl)ethyl]carbamic acid tert-butyl ester | HCID 68158397 | 81.4% |
Reaction Steps
A mixture of 3-bromo-N2-cyclopropyl-4-fluorobenzene-1,2-diamine (759 mg, 3.10 mmol), (S)-2-tertbutoxycarbonylaminopropionic acid (644 mg, 3.41 mmol), HOAt (464 mg, 3.41 mmol) and N-(3-dimethylaminopropyl)-N-ethylcarbodiimide hydrochloride (654 mg, 3.41 mmol) in DCM (20 mL) was stirred at 0° C. for 1 h. The reaction mixture was then partitioned between DCM and a saturated solution of NaHCO3. The organic fraction was dried and concentrated in vacuo. The resulting residue was purified by column chromatography (Si—PCC, gradient 0-50% EtOAc in cyclohexane) to afford the title compound (1.05 g, 81%) as a pale beige solid. LCMS (Method C): RT 3.66 min [M+H]+ 416.05
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-78ae5010312d45bd813dcf735c14ec4a |
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| Source note | uspto-grants-2014_02 |
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