Methoxyacetic Acid → HCID 178496458, compound

HRID 2042435Notes

Reaction equation

HRID 2042435 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][O:29][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][O:29][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 12251Methoxyacetic AcidHCID 178478589HCID 178478589, compound2×

Product 1

HCID 178496458HCID 178496458, compound

Procedure

The title compound, white solid (86 mg, 71%), MS (ISP) m/z=403.4 [(M+H)+], mp 169.5° 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) (132 mg, 0.3 mmol) and methoxyacetic acid.

Sources & evidence

ORD record
ord-77efb7fb2dd94e61b56f99b5eb82b379
Source dataset
uspto-grants-2013_11
Patent number
US08586579B2

Reaction notes

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