HuagongsheHuagongshe Chemistry Print Report · For research reference only
(S)-tert-Butyl 2-(4-amino-3-fluorophenyl)morpholine-4-carboxylate → (S)-2-Cyano-N-(2-fluoro-4-(morpholin-2-yl)phenyl)-6-methylisonicotinamide hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (S)-tert-Butyl 2-(4-amino-3-fluorophenyl)morpholine-4-carboxylate | HCID 68325451 | — |
| Reactant | (S)-N-(3-Chloro-4-(morpholin-2-yl)phenyl)-2-cyano-6-methylisonicotinamide hydrochloride | HCID 71086739 | — |
| Product | (S)-2-Cyano-N-(2-fluoro-4-(morpholin-2-yl)phenyl)-6-methylisonicotinamide hydrochloride | HCID 71087110 | — |
Reaction Steps
In analogy to example 83, step a) using 2-Cyano-6-methyl-isonicotinic acid (described in example 112) instead of 2-(trifluoromethyl)-4-pyridinecarboxylic acid (CAS 131747-41-6) and (−)-(S)-2-(4-Amino-3-fluoro-phenyl)-morpholine-4-carboxylic acid tert-butyl ester (preparation described in example 1-h) instead of (+)-(R)-2-(4-Amino-2-fluoro-phenyl)-morpholine-4-carboxylic acid tert-butyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09029370B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-67887a2ba4734dac9a7524a24a5fd966 |
| Source note | uspto-grants-2015_05 |