HCID 84016771, compound → HCID 118308084, compound

HRID 1750622Notes

Reaction equation

HRID 1750622 reaction equation
COC1C=CC(C)=CC=1C(N[C@H]1CCC[C@@H]1NC1C=NC(C(F)(F)F)=CN=1)=O.Cl.[F:30][C:31]([F:46])([F:45])[C:32]1[N:33]=[CH:34][C:35]([NH:38][C@H:39]2[CH2:43][CH2:42][CH2:41][C@@H:40]2[NH2:44])=[N:36][CH:37]=1.[Cl:47][C:48]1[CH:49]=[CH:50][C:51]([N:57]2[CH:61]=[CH:60][N:59]=[N:58]2)=[C:52]([CH:56]=1)[C:53](O)=[O:54]>>[Cl:47][C:48]1[CH:49]=[CH:50][C:51]([N:57]2[CH:61]=[CH:60][N:59]=[N:58]2)=[C:52]([CH:56]=1)[C:53]([NH:44][C@H:40]1[CH2:41][CH2:42][CH2:43][C@@H:39]1[NH:38][C:35]1[CH:34]=[N:33][C:32]([C:31]([F:30])([F:45])[F:46])=[CH:37][N:36]=1)=[O:54]

Participants

4

Procedure

Prepared according to the procedure for 2-methoxy-5-methyl-N-[(1S,2S)-2-{[5-(trifluoromethyl)pyrazin-2-yl]amino}cyclopentyl]benzamide (Example 37) from (1S,2S)-1-N-[5-(trifluoromethyl)pyrazin-2-yl]cyclopentane-1,2-diamine hydrochloride (Intermediate 14; 126 mg, 0.45 mmol) and 5-chloro-2-(1H-1,2,3-triazol-1-yl)benzoic acid (Intermediate 38b; 120 mg, 0.54 mmol) except this was purified by column chromatography (silica, 40-100% ethyl acetate/petrol) to afford the title compound.

Workup

  1. customPrepared
  2. customthis was purified by column chromatography (silica, 40-100% ethyl acetate/petrol)

Sources & evidence

ORD record
ord-19291a401866409996024fb382ab0654
Source dataset
uspto-grants-2015_10
Patent number
US09156829B2

Reaction notes

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