HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → HCID 86704074, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 86704073 | HCID 86704073 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86704074 | HCID 86704074 | — |
Reaction Steps
In a manner similar to the method described in Example 4, chiral 4-{[(2R,3S,4R,5S)-3-(3-chloro-2-fluoro-phenyl)-4-(4-chloro-2-fluoro-phenyl)-4-cyano-5-(2,2-dimethyl-propyl)-pyrrolidine-2-carbonyl]-amino}-3-methoxy-benzoic acid 2-((R)-2-tert-butoxycarbonylamino-propionyloxy)-ethyl ester (Example 5, 112 mg, 0.135 mmol) in methylene chloride (2 mL) was treated with trifluoroacetic acid (2 mL) to give chiral 4-{[(2R,3S,4R,5S)-3-(3-chloro-2-fluoro-phenyl)-4-(4-chloro-2-fluoro-phenyl)-4-cyano-5-(2,2-dimethyl-propyl)-pyrrolidine-2-carbonyl]-amino}-3-methoxy-benzoic acid 2-((R)-2-amino-propionyloxy)-ethyl ester as a white solid. MS (ES+) m/z calcd. for C36H39Cl2F2N4O6 [(M+H)+]: 731. found: 731.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09371280B2 |
| Source dataset | uspto-grants-2016_06 |
| ORD ID | ord-04fd1133414e40f7892af1f7b616f50e |
| Source note | uspto-grants-2016_06 |