2-Methylbutanoic Acid → HCID 178447399, compound

HRID 1260783Notes

Reaction equation

HRID 1260783 reaction equation
Cl.Cl.Cl.[O:4]1[C:8]2=[C:9]([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)[N:10]=[CH:11][CH:12]=[C:7]2[CH2:6][CH2:5]1.[CH3:28][CH:29]([CH2:33][CH3:34])[C:30](O)=[O:31]>>[O:4]1[C:8]2=[C:9]([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:30](=[O:31])[CH:29]([CH3:28])[CH2:33][CH3:34])[CH2:23][CH2:22]4)[CH2:15][CH2:14]3)[N:10]=[CH:11][CH:12]=[C:7]2[CH2:6][CH2:5]1

Participants

3

Reactant 2

HCID 83142-Methylbutanoic AcidHCID 178478590HCID 178478590, compound2×

Product 1

HCID 178447399HCID 178447399, compound

Procedure

The title compound, white solid (91 mg, 88%), MS (ISP) m/z=415.3 [(M+H)+], mp 196.5° C., was prepared in accordance with the general method of example 6 from trans-4-{2-[4-(2,3-dihydro-furo[2,3-c]pyridin-7-yl)-piperazin-1-yl]-ethyl}-cyclohexylamine trihydrochloride (intermediate B) (110 mg, 0.25 mmol) and (RS)-2-methyl-butyric acid.

Sources & evidence

ORD record
ord-9d476c6290364938ab6f5772d9ab89c8
Source dataset
uspto-grants-2013_06
Patent number
US08470828B2

Reaction notes

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