Cyclohexanecarboxylic acid → HCID 178461545, compound

HRID 730895Notes

Reaction equation

[NH2:1][C:2]1[C:7]2[NH:8][C:9]([N:11]3[CH2:16][CH2:15][N:14]([C:17]4[N:22]=[CH:21][C:20]([CH2:23][OH:24])=[CH:19][C:18]=4[Cl:25])[CH2:13][C@H:12]3[CH3:26])=[N:10][C:6]=2[CH:5]=[C:4]([C:27]([F:30])([F:29])[F:28])[CH:3]=1.[CH:31]1([C:37](O)=[O:38])[CH2:36][CH2:35][CH2:34][CH2:33][CH2:32]1>>[Cl:25][C:18]1[C:17]([N:14]2[CH2:15][CH2:16][N:11]([C:9]3[NH:8][C:7]4[C:2]([NH:1][C:37]([CH:31]5[CH2:36][CH2:35][CH2:34][CH2:33][CH2:32]5)=[O:38])=[CH:3][C:4]([C:27]([F:30])([F:29])[F:28])=[CH:5][C:6]=4[N:10]=3)[C@H:12]([CH3:26])[CH2:13]2)=[N:22][CH:21]=[C:20]([CH2:23][OH:24])[CH:19]=1

Participants

Reactant 2

HCID 7413Cyclohexanecarboxylic acid

HCID 178461542HCID 178461542, compound

Product 1

HCID 178461545HCID 178461545, compound

Procedure

{6-[(3R)-4-(7-Amino-5-trifluoromethyl-1H-benzoimidazol-2-yl)-3-methyl-piperazin-1-yl]-5-chloro-pyridin-3-yl}-methanol from (221 mg, 0.5 mmol, Example 175b) and cyclohexanecarboxylic acid (71 mg, 0.55 mmol, Aldrich) reacted under the conditions of Example 65 to give the title compound as a white solid. MS (ESI, pos. ion) m/e: 551 (M+1).

Sources & evidence

ORD record: ord-ea788d810bd84da98f22c57796262c2b
Source dataset: uspto-grants-2009_09
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07582761B2

Reaction notes

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