D-Azetidine-2-carboxylic acid → HCID 44600007, compound
Reaction equation
[F:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][C:9]=1[C:10]1[S:11][C:12]2[C:17]([N:18]=1)=[CH:16][CH:15]=[C:14]([C:19]1([C:22]3[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=3)[CH2:21][CH2:20]1)[N:13]=2)[CH:5]=O.[NH:28]1[CH2:31][CH2:30][C@@H:29]1[C:32]([OH:34])=[O:33]>>[F:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][C:9]=1[C:10]1[S:11][C:12]2[C:17]([N:18]=1)=[CH:16][CH:15]=[C:14]([C:19]1([C:22]3[CH:23]=[CH:24][CH:25]=[CH:26][CH:27]=3)[CH2:20][CH2:21]1)[N:13]=2)[CH2:5][N:28]1[CH2:31][CH2:30][C@@H:29]1[C:32]([OH:34])=[O:33]Participants
3
Procedure
Reaction of 3-fluoro-4-(5-(1-phenylcyclopropyl)thiazolo[5,4-b]pyridin-2-yl)benzaldehyde (106.1 mg, 0.283 mmol) and (R)-azetidine-2-carboxylic acid (86 mg, 0.850 mmol) according to Reference R and the general procedure for reductive amination gave (R)-1-(3-fluoro-4-(5-(1-phenylcyclopropyl)thiazolo[5,4-b]pyridin-2-yl)benzyl)azetidine-2-carboxylic acid as a brown solid. MS (ESI) m/z: Calculated: 459.1; Observed: 460.1 (M++1).
Sources & evidence
- ORD record
- ord-46ffb42057974dc99220d6a4a68f5f26
- Source dataset
- uspto-grants-2010_11
- Patent number
- US07842685B2
Reaction notes
Loading…