HuagongsheHuagongshe Chemistry Print Report · For research reference only
(S)-cyclopentyl 2-amino-4-methylpentanoate → Cyclopentyl N-[2-(4-{6-amino-5-[(4-fluorophenyl)carbonyl]-2-oxopyridin-1(2H)-yl}phenyl)ethyl]-L-leucinate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (S)-cyclopentyl 2-amino-4-methylpentanoate | HCID 53718217 | — |
| Reactant | Methanesulfonic acid 2-{4-[6-amino-5-(4-fluoro-benzoyl)-2-oxo-2H-pyridin-1-yl]-phenyl}-ethyl ester | HCID 58608538 | — |
| Product | Cyclopentyl N-[2-(4-{6-amino-5-[(4-fluorophenyl)carbonyl]-2-oxopyridin-1(2H)-yl}phenyl)ethyl]-L-leucinate | HCID 57658470 | — |
Reaction Steps
From Intermediate 4J and L-Leucine cyclopentyl ester (Intermediate 8). LC/MS: m/z 534 [M+H]+. 1H NMR (300 MHz, DMSO-d6) δ: 8.47 (1H, d, J=7.7 Hz), 7.56 (2H, m), 7.45 (1H, d, J=9.6 Hz), 7.38-7.24 (4H, m), 7.15 (2H, m), 5.69 (1H, d, J=9.8 Hz), 5.09 (1H, t, J=5.3 Hz), 4.63 (2H, m), 4.31 (1H, m), 1.84-1.79 (2H, m), 1.66-1.53 (9H, m), 0.92-0.86 (6H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08044211B2 |
| Source dataset | uspto-grants-2011_10 |
| ORD ID | ord-b92f1569b80744cf80561c210792a5fd |
| Source note | uspto-grants-2011_10 |