HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 76021605, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 76021602 | HCID 76021602 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 76021605 | HCID 76021605 | — |
Reaction Steps
In a manner similar to the method described in Example 27, rac-(2′S,3′S,4′S)-6-chloro-2′-(3-chloro-2-fluoro-phenyl)-4′-(2,2-dimethyl-propyl)-2-oxo-1,2-dihydro-spiro[indole-3,3′-pyrrolidine]-1′-carboxylic acid (piperidin-4-ylmethyl)-amide trifluoroacetic acid prepared in Example 44 (35 mg, 0.05 mmol) was reacted with triethylamine and methanesulfonyl chloride (6.5 mg, 0.06 mmol) in dichloromethane to give rac-(2′S,3′S,4′S)-6-chloro-2′-(3-chloro-2-fluoro-phenyl)-4′-(2,2-dimethyl-propyl)-2-oxo-1,2-dihydro-spiro[indole-3,3′-pyrrolidine]-1′-carboxylic acid (1-methanesulfonyl-piperidin-4-ylmethyl)-amide as a white solid (Yield, 13 mg, 39%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08288431B2 |
| Source dataset | uspto-grants-2012_10 |
| ORD ID | ord-3e760999b63245a5b4d18dfb94c5b800 |
| Source note | uspto-grants-2012_10 |