5-(1,1-Difluoroethyl)pyrazine-2-carboxylic acid → N-(3-((4aS,5S,7aS)-2-amino-5-(trifluoromethyl)-4a,5,7,7a-tetrahydro-4H-furo[3,4-d][1,3]thiazin-7a-yl)-4-fluorophenyl)-5-(1,1-difluoroethyl)pyrazine-2-carboxamide
Reaction equation
C(OC(=O)[NH:7][C:8]1[S:9][CH2:10][C@@H:11]2[C@@H:16]([C:17]([F:20])([F:19])[F:18])[O:15][CH2:14][C@:12]2([C:21]2[CH:26]=[C:25]([NH2:27])[CH:24]=[CH:23][C:22]=2[F:28])[N:13]=1)(C)(C)C.[F:30][C:31]([C:34]1[N:35]=[CH:36][C:37]([C:40](O)=[O:41])=[N:38][CH:39]=1)([F:33])[CH3:32]>>[NH2:7][C:8]1[S:9][CH2:10][C@@H:11]2[C@@H:16]([C:17]([F:19])([F:20])[F:18])[O:15][CH2:14][C@:12]2([C:21]2[CH:26]=[C:25]([NH:27][C:40]([C:37]3[CH:36]=[N:35][C:34]([C:31]([F:33])([F:30])[CH3:32])=[CH:39][N:38]=3)=[O:41])[CH:24]=[CH:23][C:22]=2[F:28])[N:13]=1Participants
3
Reactant 2
Product 1
Procedure
Synthesized from tert-butyl[(4aS,5S,7aS)-7a-(5-amino-2-fluorophenyl)-5-trifluoromethyl-4a,5,7,7a-tetrahydro-4H-furo[3,4-d][1,3]thiazin-2-yl]carbamate and 5-(1,1-difluoroethyl)pyrazine-2-carboxylic acid according to the general procedure. 1H NMR (600 MHz, CDCl3) δ ppm 2.03 (t, J=18.8 Hz, 3 H), 2.82 (d, J=12.0 Hz, 1 H), 3.14 (d, J=12.4 Hz, 1 H), 3.35-3.46 (m, 1 H), 3.77-4.07 (m, 1 H), 4.20-4.93 (m, 4 H), 7.08 (dd, J=11.7, 9.0 Hz, 1 H), 7.56 (d, J=4.5 Hz, 1 H), 7.80-7.93 (m, 1 H), 8.87 (s, 1 H), 9.43 (s, 1 H), 9.59 (br. s., 1 H)
Sources & evidence
- ORD record
- ord-99baeb59c8b7494081c05ca080dfa7be
- Source dataset
- uspto-grants-2015_01
- Patent number
- US08940734B2
Reaction notes
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