Cyclopropanemethanamine → HCID 57377807, compound

HRID 1258933Notes

Reaction equation

HRID 1258933 reaction equation
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[N:8]1[C:12]([C:13]2[N:14]=[CH:15][N:16]([C:18]3[CH:26]=[CH:25][C:21]([C:22]([OH:24])=O)=[CH:20][N:19]=3)[CH:17]=2)=[C:11]([CH3:27])[N:10]=[N:9]1.[NH2:28][CH2:29][CH:30]1[CH2:32][CH2:31]1>>[CH:30]1([CH2:29][NH:28][C:22](=[O:24])[C:21]2[CH:25]=[CH:26][C:18]([N:16]3[CH:17]=[C:13]([C:12]4[N:8]([C:3]5[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=5[F:1])[N:9]=[N:10][C:11]=4[CH3:27])[N:14]=[CH:15]3)=[N:19][CH:20]=2)[CH2:32][CH2:31]1

Participants

3

Reactant 2

HCID 75646CyclopropanemethanamineHCID 679551606-(4-(1-(2-Fluorophenyl)-4-methyl-1H-1,2,3-triazol-5-yl)-1H-imidazol-1-yl)nicotinic acid

Product 1

HCID 57377807HCID 57377807, compoundYield 47%

Procedure

As described for example 43c, 6-(4-(1-(2-fluorophenyl)-4-methyl-1H-1,2,3-triazol-5-yl)-1H-imidazol-1-yl)nicotinic acid (74 mg, 0.203 mmol) was converted, using aminomethylcyclopropane instead of isopropylamine, to the title compound (40 mg, 47%) which was obtained as a white foam after purification by chromatography (reverse phase HPLC). MS: m/e=418.3 [M+H]+.

Sources & evidence

ORD record
ord-f21dd19c16954c11a4d92a2b75c4cabb
Source dataset
uspto-grants-2013_06
Patent number
US08466181B2

Reaction notes

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