HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 18187872, compound → HCID 57040067, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 18187872 | HCID 18187872 | — |
| Reactant | alpha-(R)-(3-(R)-formyl-4-(S)-phenylpyrrolidin-1-yl)-cyclohexaneacetic acid 4-methoxybenzyl ester | HCID 53654320 | — |
| Solvent | Dichloromethane methanol | HCID 21226129 | — |
| Product | HCID 57040067 | HCID 57040067 | 97% |
Reaction Steps
The title compound was prepared from 42 mg (0.096 mmol) of 2-(R)-(3-(R)-formyl-4-(S)-phenylpyrrolidin-1-yl)-2-(cyclohexyl)acetic acid, (4-methoxy)benzyl ester (from EXAMPLE 33, Step E) and 36 mg (0.18 mmol) of 4-(2-pyridylpropyl)piperidine.2 TFA (from EXAMPLE 72, Step B) using a procedure analogous to that described in EXAMPLE 71, Step A. Flash chromatography using 25:1 v/v CH2Cl2/MeOH provided 58 mg (97%) of the title compound: 1H NMR (500 MHz) δ 0.94-3.28(35H), 3.82 (s, 3H), 5.11 (ABq, J=11.9, 2H), 6.88-7.35 (11H), 7.58-7.61 (m, 1H), 8.52 (d, J=4.1, 1H); ESI-MS 624 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06265434B1 |
| Source dataset | uspto-grants-2001_07 |
| ORD ID | ord-42ad73b089f74a2cb0767b2aab4b0890 |
| Source note | uspto-grants-2001_07 |