Isovaleric Acid → HCID 178447392, compound

HRID 2042464Notes

Reaction equation

HRID 2042464 reaction equation
Cl.Cl.Cl.[O:4]1[C:12]2[CH:11]=[CH:10][N:9]=[C:8]([N:13]3[CH2:18][CH2:17][N:16]([CH2:19][CH2:20][C@H:21]4[CH2:26][CH2:25][C@H:24]([NH2:27])[CH2:23][CH2:22]4)[CH2:15][CH2:14]3)[C:7]=2[CH2:6][CH2:5]1.[CH3:28][CH:29]([CH3:34])[CH2:30][C:31](O)=[O:32]>>[O:4]1[C:12]2[CH:11]=[CH:10][N:9]=[C:8]([N:13]3[CH2:18][CH2:17][N:16]([CH2:19][CH2:20][C@H:21]4[CH2:26][CH2:25][C@H:24]([NH:27][C:31](=[O:32])[CH2:30][CH:29]([CH3:34])[CH3:28])[CH2:23][CH2:22]4)[CH2:15][CH2:14]3)[C:7]=2[CH2:6][CH2:5]1

Participants

3

Reactant 2

HCID 10430Isovaleric AcidHCID 178478589HCID 178478589, compound2×

Product 1

HCID 178447392HCID 178447392, compound

Procedure

The title compound, white solid (84 mg, 81%), MS (ISP) m/z=415.4 [(M+H)+], mp 202.5° C., was prepared in accordance with the general method of example 32 from trans-4-{2-[4-(2,3-dihydrofuro[3,2-c]pyridin-4-yl)-piperazin-1-yl]-ethyl}-cyclohexanamine trihydrochloride (intermediate C) (110 mg, 0.25 mmol) and 3-methyl-butyric acid.

Sources & evidence

ORD record
ord-73edaa30d0a144f387f889e7d43d6b65
Source dataset
uspto-grants-2013_11
Patent number
US08586579B2

Reaction notes

Loading…