(R)-Homo-beta-alanine hydrochloride → HCID 67111813, compound

HRID 1177604Notes

Reaction equation

HRID 1177604 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.[ClH:28].[NH2:29][C@H:30]([CH3:35])[CH2:31][C:32]([OH:34])=[O:33]>>[ClH:28].[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][NH:29][C@H:30]([CH3:35])[CH2:31][C:32]([OH:34])=[O:33]

Participants

3

Reactant 2

HCID 22982782(R)-Homo-beta-alanine hydrochlorideHCID 591749073-Fluoro-4-(5-(1-phenylcyclopropyl)thiazolo[5,4-b]pyridin-2-yl)benzaldehyde

Product 1

HCID 67111813HCID 67111813, compound

Procedure

Reaction of 3-fluoro-4-(5-(1-phenylcyclopropyl)thiazolo[5,4-b]pyridin-2-yl)benzaldehyde (0.040 g, 0.11 mmol) and (R)-3-aminobutanoic acid hydrochloride (0.056 g, 0.40 mmol) according to Reference R and general procedure for reductive amination afforded (R)-3-(3-fluoro-4-(5-(1-phenylcyclopropyl)thiazolo[5,4-b]pyridin-2-yl)benzylamino)butanoic acid hydrochloride. MS (ESI) m/z: calculated: 461.2; Observed: 462.1 (M++1).

Sources & evidence

ORD record
ord-fa87dc09fb654121a5d004c59d97fd89
Source dataset
uspto-grants-2010_11
Patent number
US07842685B2

Reaction notes

Loading…