HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → HCID 86757030, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Anisole | HCID 7519 | — |
| Reactant | HCID 86757031 | HCID 86757031 | — |
| Product | HCID 86757030 | HCID 86757030 | 104.3% |
Reaction Steps
The title compound was prepared from 19 mg of α-(R)-(3-(S)-((4-(imidazo[1,2-a]pyridin-2-yl)-piperidine-1-yl)methyl)-4-(S)-(3-fluorophenyl)pyrrolidin-1-yl)-cyclobutylpropanoic acid, 4-methoxy-benzyl ester (from Step C), 2 mL of TFA and 0.2 mL of anisole, using a procedure analogous to that described in Example 235, Step D to provide 16 mg of the title compound as a foamy solid. 1H NMR (500 MHz, CD3OD): δ1.45-1.64 (m, 6H), 1.83-2.04 (m, 6H), 2.30(t, J=14.2 Hz, 3H), 2.68-3.85(m, 12H), 6.93 (t, J=6.3 Hz, 1H), 7.27 (d, J=6.7 Hz, 2H), 7.35 (t, J=6.7 Hz, 1H), 7.45 (dd, J=13.6, 6.3Hz, 1H), 7.49 (d, J=13.5 Hz, 1H), 7.67 (s, 1H), 8.38 (d, J=6.9 Hz, 1H). ESI-MS 505 (M+H); HPLC A 2.21 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06248755B1 |
| Source dataset | uspto-grants-2001_06 |
| ORD ID | ord-e30058f44d5f49e98ec8cb3adf146095 |
| Source note | uspto-grants-2001_06 |