2-Amino-2-methyl-1-propanol → HCID 49801310, compound

HRID 1807525Notes

Reaction equation

HRID 1807525 reaction equation
CO[C:3](=[O:24])[C:4]1[CH:9]=[CH:8][C:7]([O:10][CH2:11][C:12]2[C:13]([CH:18]3[CH2:23][CH2:22][CH2:21][CH2:20][CH2:19]3)=[N:14][O:15][C:16]=2[CH3:17])=[N:6][CH:5]=1.[NH2:25][C:26]([CH3:30])([CH3:29])[CH2:27][OH:28]>>[CH:18]1([C:13]2[C:12]([CH2:11][O:10][C:7]3[CH:8]=[CH:9][C:4]([C:3]([NH:25][C:26]([CH3:30])([CH3:29])[CH2:27][OH:28])=[O:24])=[CH:5][N:6]=3)=[C:16]([CH3:17])[O:15][N:14]=2)[CH2:19][CH2:20][CH2:21][CH2:22][CH2:23]1

Participants

3

Reactant 2

HCID 118072-Amino-2-methyl-1-propanolHCID 66643566HCID 66643566, compound

Product 1

HCID 49801310HCID 49801310, compoundYield 58%

Procedure

As described for example 31e, 6-(3-cyclohexyl-5-methyl-isoxazol-4-ylmethoxy)-nicotinic acid methyl ester (708 mg, 1.5 mmol) was converted, using 2-amino-2-methyl-1-propanol instead of isopropylamine, to the title compound (340 mg, 58%) which was obtained as a white solid after purification by chromatography (silica, 0 to 4% methanol in dichloromethane). MS: m/e=388.4 [M+H]+.

Sources & evidence

ORD record
ord-2e012bd31d214cca81253198592070cc
Source dataset
uspto-grants-2013_01
Patent number
US08357703B2

Reaction notes

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