HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl L-valinate hydrochloride → HCID 10712597, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl L-valinate hydrochloride | HCID 87181 | — |
| Reactant | 4-(4-Oxopiperidin-1-yl)benzoic acid | HCID 22064022 | — |
| Product | HCID 10712597 | HCID 10712597 | — |
Reaction Steps
The title compound was prepared from 4-(4-oxo-piperidine-1-yl)-benzoic acid (which was obtained in Example 151) and L-valine ethyl ester hydrochloride according to the procedure of Example 154 as a pale yellowish solid; 1H NMR (300 MHz, DMSO-d6) δ 0.93 (d, J=6.8 Hz, 3H), 0.97 (d, J=6.8 Hz, 3H), 1.20 (t, J=7.1 Hz, 3H), 2.10-2.30 (m, 1H), 2.43 (t, J=6.0 Hz, 4H), 3.72 (t, J=6.0 Hz, 4H), 4.00-4.30 (m, 4H), 4.46 (t, J=5.1 Hz, 1H), 7.05 (d, J=8.9 Hz, 2H), 7.82 (d, J=8.9 Hz, 2H), 8.21 (d, J=7.9 Hz, 1H); MS (ES) m/z: 347.3 (MH+); HRMS Calcd. for C19H26N2O4 (M+): 346.1892. Found: 346.1896.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06525202B2 |
| Source dataset | uspto-grants-2003_02 |
| ORD ID | ord-704ab50a26494e8695118faa41884de1 |
| Source note | uspto-grants-2003_02 |