4-Pyridinemethanamine → 4-methyl-2-(2-oxo-3-(4,4,4-trifluorobutyl)imidazolidin-1-yl)-N-(pyridin-4-ylmethyl)thiazole-5-carboxamide

HRID 554987Notes

Reaction equation

HRID 554987 reaction equation
FC1C=C(CN)C=NC=1.[N:10]1[CH:15]=[CH:14][C:13]([CH2:16][NH2:17])=[CH:12][CH:11]=1.[CH3:18][C:19]1[N:20]=[C:21]([N:27]2[CH2:31][CH2:30][N:29]([CH2:32][CH2:33][CH2:34][C:35]([F:38])([F:37])[F:36])[C:28]2=[O:39])[S:22][C:23]=1[C:24](O)=[O:25]>>[CH3:18][C:19]1[N:20]=[C:21]([N:27]2[CH2:31][CH2:30][N:29]([CH2:32][CH2:33][CH2:34][C:35]([F:36])([F:37])[F:38])[C:28]2=[O:39])[S:22][C:23]=1[C:24]([NH:17][CH2:16][C:13]1[CH:14]=[CH:15][N:10]=[CH:11][CH:12]=1)=[O:25]

Participants

4

Reactant 3

HCID 773174-PyridinemethanamineHCID 45116207(5-Fluoropyridin-3-yl)methanamineHCID 579198994-Methyl-2-(2-oxo-3-(4,4,4-trifluorobutyl)imidazolidin-1-yl)thiazole-5-carboxylic acid

Product 1

HCID 579199944-methyl-2-(2-oxo-3-(4,4,4-trifluorobutyl)imidazolidin-1-yl)-N-(pyridin-4-ylmethyl)thiazole-5-carboxamideYield 42%

Procedure

Following the procedure as describe in Example 12, making variations as required to replace (5-fluoropyridin-3-yl)methanamine with pyridin-4-ylmethanamine to react with 4-methyl-2-(2-oxo-3-(4,4,4-trifluorobutyl)imidazolidin-1-yl)thiazole-5-carboxylic acid in place of 2-(3-(cyclopropylmethyl)-2-oxoimidazolidin-1-yl)-4-methylthiazole-5-carboxylic acid, the title compound was obtained as a colorless solid in 42% yield: mp 178-181° C. (dichloromethane/hexanes); 1H NMR (300 MHz, CDCl3) δ 8.55 (s, 2H), 7.24-7.22 (m, 2H), 6.20-6.16 (m, 1H), 4.57 (d, J=5.9 Hz, 2H), 4.16-4.10 (m, 2H), 3.63-3.58 (m, 2H), 3.41-3.39 (m, 2H), 2.61 (s, 3H), 2.19-2.10 (m, 2H), 1.91-1.83 (m, 2H); MS (ES+) m/z 428.2 (M+1).

Sources & evidence

ORD record
ord-d9e185fc0972463e906a42fdf3463459
Source dataset
uspto-grants-2011_11
Patent number
US08049016B2

Reaction notes

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