5-(1,1-Difluoroethyl)pyrazine-2-carboxylic acid → 5-(1,1-Difluoro-ethyl)-pyrazine-2-carboxylic acid [3-((4S,4aR,7aR)-2-amino-5,5-difluoro-4-methyl-4,4a,5,6,7,7a-hexahydro-cyclopenta[e][1,3]oxazin-4-yl)-4-fluoro-phenyl]-amide

HRID 710196Notes

Reaction equation

HRID 710196 reaction equation
[NH2:1][C:2]1[CH:3]=[CH:4][C:5]([F:21])=[C:6]([C@:8]2([CH3:20])[C@H:13]3[C:14]([F:18])([F:17])[CH2:15][CH2:16][C@H:12]3[O:11][C:10]([NH2:19])=[N:9]2)[CH:7]=1.[F:22][C:23]([C:26]1[N:27]=[CH:28][C:29]([C:32](O)=[O:33])=[N:30][CH:31]=1)([F:25])[CH3:24]>>[NH2:19][C:10]1[O:11][C@@H:12]2[CH2:16][CH2:15][C:14]([F:17])([F:18])[C@@H:13]2[C@:8]([C:6]2[CH:7]=[C:2]([NH:1][C:32]([C:29]3[CH:28]=[N:27][C:26]([C:23]([F:25])([F:22])[CH3:24])=[CH:31][N:30]=3)=[O:33])[CH:3]=[CH:4][C:5]=2[F:21])([CH3:20])[N:9]=1

Participants

3

Procedure

The coupling of (4S,4aR,7aR)-4-(5-amino-2-fluoro-phenyl)-5,5-difluoro-4-methyl-4,4a,5,6,7,7a-hexahydro-cyclopenta[e][1,3]oxazin-2-ylamine (intermediate XIIIa-1) and 5-(1,1-difluoro-ethyl)-pyrazine-2-carboxylic acid (CAS 1262803-63-315) following procedure Q yielded the title compound as a white solid (52% yield). MS: m/z=470.3 [M+H]+.

Sources & evidence

ORD record
ord-c348c070013f401e87eed95b121de236
Source dataset
uspto-grants-2015_11
Patent number
US09181232B2

Reaction notes

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