HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 243086Generated: October 30, 2026
Tert-butoxycarbonylalanine → HCID 178462194, compound
https://huagongshe.com/reaction/243086
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tert-butoxycarbonylalanine | HCID 85082 | — |
| Reactant | HOAt | HCID 181649 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | HCID 178507657 | HCID 178507657 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178462194 | HCID 178462194 | — |
Reaction Steps
A mixture of N2-(trans-3-benzyloxycyclobutyl)-4-fluoro-benzene-1,2-diamine (1.73 g, 2.55 mmol), (S)-2-tertbutoxycarbonylaminopropionic acid (0.54 g, 2.81 mmol) and HOAt (0.38 g, 2.81 mmol) in DCM (20 mL) were cooled to 0° C. under nitrogen atmosphere. To this mixture N-(3-dimethylaminopropyl)-N-ethylcarbodiimide hydrochloride (0.54 g, 2.81 mmol) was added portion wise and the reaction mixture was stirred at RT for 1 h. The reaction mixture allowed to warm to RT then partitioned between DCM (30 mL) and 10% aqueous citric acid (20 mL). The organic layer was washed with brine (20 mL), dried (MgSO4) and concentrated in vacuo and the resulting residue purified by column chromatography (Si—PCC, gradient 0-50% EtOAc in cyclohexane) to afford the title compound as a off-white gum, which solidified on standing (0.88 g, 75%). NMR: 328289. LCMS (Method B): RT 3.85 min [M+H]+ 458.
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-772a8c73e9db4872b26723aea794dc7b |
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| Source note | uspto-grants-2014_02 |
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