5-fluoro-2-(2H-1,2,3-triazol-2-yl)benzoic acid → 5-Fluoro-2-(2H-1,2,3-triazol-2-yl)-N-[(1S,2S)-2-{[5-(trifluoromethyl)pyrazin-2-yl]amino}cyclopentyl]benzamide
Reaction equation
N1(C2C=CC=CC=2C(N[C@H]2CCC[C@@H]2NC2C=NC(C(F)(F)F)=CN=2)=O)C=CC=N1.Cl.[F:32][C:33]([F:48])([F:47])[C:34]1[N:35]=[CH:36][C:37]([NH:40][C@H:41]2[CH2:45][CH2:44][CH2:43][C@@H:42]2[NH2:46])=[N:38][CH:39]=1.[F:49][C:50]1[CH:51]=[CH:52][C:53]([N:59]2[N:63]=[CH:62][CH:61]=[N:60]2)=[C:54]([CH:58]=1)[C:55](O)=[O:56]>>[F:49][C:50]1[CH:51]=[CH:52][C:53]([N:59]2[N:63]=[CH:62][CH:61]=[N:60]2)=[C:54]([CH:58]=1)[C:55]([NH:46][C@H:42]1[CH2:43][CH2:44][CH2:45][C@@H:41]1[NH:40][C:37]1[CH:36]=[N:35][C:34]([C:33]([F:32])([F:47])[F:48])=[CH:39][N:38]=1)=[O:56]Participants
4
Reactant 3
Product 1
Procedure
Prepared according to the procedure for 2-(1H-pyrazol-1-yl)-N-[(1S,2S)-2-{[5-(trifluoromethyl)pyrazin-2-yl]amino}cyclopentyl]benzamide (Example 31) from (1S,2S)-1-N-[5-(trifluoromethyl)pyrazin-2-yl]cyclopentane-1,2-diamine hydrochloride (Intermediate 14, 213 mg, 0.75 mmol) and 5-fluoro-2-(2H-1,2,3-triazol-2-yl)benzoic acid (Intermediate 8; 172 mg, 0.83 mmol) except this was then purified by column chromatography (silica, 0-100% ethyl acetate/petrol) to afford the title compound.
Workup
- customPrepared
- customthis was then purified by column chromatography (silica, 0-100% ethyl acetate/petrol)
Sources & evidence
- ORD record
- ord-69ff5368cf9d488a81fcb4aada1e71ce
- Source dataset
- uspto-grants-2015_10
- Patent number
- US09156829B2
Reaction notes
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