HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,5-Bis(2,2,2-trifluoroethoxy)benzene-1-sulfonyl chloride → (4R)-1-[1-{[2,5-bis (2,2,2-trifluoroethoxy)phenyl]sulfonyl}-5-chloro-3-(2-methoxyphenyl)-2-oxo-2,3-dihydro-1H-in dol-3-yl]-4-hydroxy-N,N-dimethyl-L-prolinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,5-Bis(2,2,2-trifluoroethoxy)benzene-1-sulfonyl chloride | HCID 2736077 | — |
| Reactant | (2S,4R)-1-(5-Chloro-3-(2-methoxyphenyl)-2-oxoindolin-3-YL)-4-hydroxy-N,N-dimethylpyrrolidine-2-carboxamide | HCID 67044068 | — |
| Product | (4R)-1-[1-{[2,5-bis (2,2,2-trifluoroethoxy)phenyl]sulfonyl}-5-chloro-3-(2-methoxyphenyl)-2-oxo-2,3-dihydro-1H-in dol-3-yl]-4-hydroxy-N,N-dimethyl-L-prolinamide | HCID 59867949 | 66.8% |
Reaction Steps
With 100 mg of (4R)-1-[5-chloro-3-(2-methoxyphenyl)-2-oxo-2,3-dihydro-1H-indol-3-yl]-4-hydroxy-N,N-dimethyl-L-prolinamide (levorotatory isomer), which is the compound described in Preparation 3.2 (Isomer B) of the brochure Publication No. WO01/55130, and 89 mg of 2,5-bis (2,2,2-trifluoroethoxy)benzene sulfonyl chloride as starting materials, 119 mg of the title compound (colorless amorphous) was obtained by a similar method to Example 2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08030499B2 |
| Source dataset | uspto-grants-2011_10 |
| ORD ID | ord-8348b5f92fa34fa1a6279c94037de063 |
| Source note | uspto-grants-2011_10 |