Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828357Generated: November 1, 2026

(2S, 3S)-3-(5-chloroindole-2-carbonylamino)-2-methyl-2,3-dihydro-1,5-benzoxazepin-4 (5H)-one → (2S, 3R)-3-(5-chloroindole-2-carbonylamino)-2-methyl-2,3-dihydro-1,5-benzoxazepin-4 (5H)-one

https://huagongshe.com/reaction/1828357

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2S, 3S)-3-(5-chloroindole-2-carbonylamino)-2-methyl-2,3-dihydro-1,5-benzoxazepin-4 (5H)-oneHCID 10067708—
Reactant(2S, 3S)-3-amino-2-methyl-2,3-dihydro-1,5-benzoxazepin-4(5H)-one trifluoroacetate saltHCID 69195761—
ReactantHCID 69196397HCID 69196397—
Product(2S, 3R)-3-(5-chloroindole-2-carbonylamino)-2-methyl-2,3-dihydro-1,5-benzoxazepin-4 (5H)-oneHCID 11559723—

Reaction Steps

The title compound was prepared from (2S,3R)-3-amino-2-methyl-2,3-dihydro-1,5-benzoxazepin-4(5H)-one trifluoroacetate salt by the procedures described for the preparation of (2S,3S)-3-(5-chloroindole-2-carbonylamino)-2-methyl-2,3-dihydro-1,5-benzoxazepin-4(5H)-one (Example 22) from (2S,3S)-3-amino-2-methyl-2,3-dihydro-1,5-benzoxazepin-4(5H)-one trifluoroacetate salt. HPLC/MS [M+H]+, 370.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07057046B2
Source datasetuspto-grants-2006_06
ORD IDord-30647d61ce9648eaaac37b9c952db602
Source noteuspto-grants-2006_06