L-Lactic Acid → HCID 69507874, compound
Reaction equation
Cl.[NH2:2][C@@H:3]1[C:9](=[O:10])[N:8]([CH3:11])[C:7]2[CH:12]=[CH:13][CH:14]=[CH:15][C:6]=2[C:5]2[CH:16]=[CH:17][CH:18]=[CH:19][C:4]1=2.[C:20](O)(=[O:24])[C@H:21]([CH3:23])[OH:22]>>[OH:22][C@@H:21]([CH3:23])[C:20]([NH:2][C@@H:3]1[C:9](=[O:10])[N:8]([CH3:11])[C:7]2[CH:12]=[CH:13][CH:14]=[CH:15][C:6]=2[C:5]2[CH:16]=[CH:17][CH:18]=[CH:19][C:4]1=2)=[O:24]Participants
3
Procedure
The title compound, MS: m/e=311.3 (M+H+), was prepared in analogy to example 1a) from (−)-(S)-7-amino-5-methyl-5H,7H-dibenzo[b,d]azepin-6-one hydrochloride and L-(+)-lactic acid.
Sources & evidence
- ORD record
- ord-84b79a1039394323be456e6b7aff4dc3
- Source dataset
- uspto-grants-2007_01
- Patent number
- US07166587B2
Reaction notes
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