HCID 21072482, compound → HCID 24875755, compound
Reaction equation
[NH2:1][C@@H:2]1[C:8](=[O:9])[N:7]([CH2:10][CH:11]([OH:16])[C:12]([F:15])([F:14])[F:13])[C:6]2[CH:17]=[CH:18][CH:19]=[CH:20][C:5]=2[C:4]2[CH:21]=[CH:22][CH:23]=[CH:24][C:3]1=2.[CH3:25][C:26]([CH3:41])([C:30]([NH:32][CH2:33][C:34]([F:40])([F:39])[C:35]([F:38])([F:37])[F:36])=[O:31])[C:27](O)=[O:28]>>[CH3:25][C:26]([CH3:41])([C:30]([NH:32][CH2:33][C:34]([F:39])([F:40])[C:35]([F:36])([F:38])[F:37])=[O:31])[C:27]([NH:1][C@@H:2]1[C:8](=[O:9])[N:7]([CH2:10][CH:11]([OH:16])[C:12]([F:15])([F:13])[F:14])[C:6]2[CH:17]=[CH:18][CH:19]=[CH:20][C:5]=2[C:4]2[CH:21]=[CH:22][CH:23]=[CH:24][C:3]1=2)=[O:28]Participants
3
Procedure
Using (S)-7-amino-5-(3,3,3-trifluoro-2-hydroxy-propyl)-5H,7H-dibenzo[b,d]azepin-6-one and 2,2-dimethyl-N-(2,2,3,3,3-pentafluoro-propyl)-malonamic acid, the title compound was prepared in the same manner as example 1c (87%). White solid. MS: m/e=582(M+H+).
Sources & evidence
- ORD record
- ord-a73c9099777e46229813de841f7fa4c5
- Source dataset
- uspto-grants-2008_09
- Patent number
- US07425551B2
Reaction notes
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