6-Morpholinonicotinic Acid → HCID 178523652, compound

HRID 1409924Notes

Reaction equation

HRID 1409924 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][N:34]=2)[CH2:32][CH2:31][O: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[CH2:28][CH2:29][O:30][CH2:31][CH2:32]4)=[N:34][CH:35]=3)[CH2:24][CH2:25]2)=[CH:4]1

Participants

3

Reactant 2

HCID 27764606-Morpholinonicotinic AcidHCID 178478713HCID 178478713, compound2×

Product 1

HCID 178523652HCID 178523652, compound

Procedure

The title compound, light yellow solid (81 mg, 63%), MS (ISP) m/z=517.3 [(M+H)+], mp 215° 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 6-morpholin-4-yl-nicotinic acid.

Sources & evidence

ORD record
ord-a0c564488e3d42be9a70d6c767862e96
Source dataset
uspto-grants-2014_12
Patent number
US08921397B2

Reaction notes

Loading…