4-(Piperidin-1-yl)benzoic acid → HCID 178523649, compound

HRID 1409910Notes

Reaction equation

HRID 1409910 reaction equation
Cl.Cl.[O:3]1[C:8]2=[CH:9][CH:10]=[CH:11][C:7]2=[CH:6][C:5]([CH:12]2[CH2:17][CH2:16][CH2:15][CH2:14][N:13]2[CH2:18][CH2:19][C@H:20]2[CH2:25][CH2:24][C@H:23]([NH2:26])[CH2:22][CH2:21]2)=[CH:4]1.[N:27]1([C:33]2[CH:41]=[CH:40][C:36]([C:37](O)=[O:38])=[CH:35][CH:34]=2)[CH2:32][CH2:31][CH2:30][CH2:29][CH2:28]1>>[O:3]1[C:8]2=[CH:9][CH:10]=[CH:11][C:7]2=[CH:6][C:5]([CH:12]2[CH2:17][CH2:16][CH2:15][CH2:14][N:13]2[CH2:18][CH2:19][C@H:20]2[CH2:21][CH2:22][C@H:23]([NH:26][C:37](=[O:38])[C:36]3[CH:40]=[CH:41][C:33]([N:27]4[CH2:32][CH2:31][CH2:30][CH2:29][CH2:28]4)=[CH:34][CH:35]=3)[CH2:24][CH2:25]2)=[CH:4]1

Participants

3

Reactant 2

HCID 7645994-(Piperidin-1-yl)benzoic acidHCID 178478713HCID 178478713, compound2×

Product 1

HCID 178523649HCID 178523649, compound

Procedure

The title compound, off-white solid (95 mg, 72%), MS (ISP) m/z=514.4 [(M+H)+], mp 221° C., was prepared in accordance with the general method of example 1 from trans-4-[2-(4-benzofuran-3-yl-piperidin-1-yl)-ethyl]-cyclohexylamine dihydrochloride (intermediate A) (100 mg, 0.25 mmol) and 4-piperidin-1-yl-benzoic acid.

Sources & evidence

ORD record
ord-5a4b29bb67724ecdade51ae1935b38a6
Source dataset
uspto-grants-2014_12
Patent number
US08921397B2

Reaction notes

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