Methyl 3,3-dimethoxypropionate → HCID 178495582, compound

HRID 2042501Notes

Reaction equation

HRID 2042501 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][CH:30]([O:36][CH3:37])[CH2:31][C:32](OC)=[O:33]>>[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:32](=[O:33])[CH2:31][CH:30]([O:36][CH3:37])[O:29][CH3:28])[CH2:23][CH2:22]4)[CH2:15][CH2:14]3)[C:7]=2[CH2:6][CH2:5]1

Participants

3

Procedure

The title compound, white solid (101 mg, 91%), MS (ISP) m/z=447.4 [(M+H)+], mp 220° C., was prepared in accordance with the general method of example 2 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 methyl 3,3-dimethoxy-propanoate.

Sources & evidence

ORD record
ord-5a2c7b6e74164bc89eb6b08abc23e641
Source dataset
uspto-grants-2013_11
Patent number
US08586579B2

Reaction notes

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