4-(Methylsulfonyl)benzyl Bromide → 2-[1-(4-methanesulfonyl-benzyl)-1H-pyrazol-3-yl]-4-methyl-thiazole-5-carboxylic acid (pyridin-3-ylmethyl)amide

HRID 1879197Notes

Reaction equation

HRID 1879197 reaction equation
[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([CH2:7][NH:8][C:9]([C:11]2[S:15][C:14]([C:16]3[NH:17][N:18]=[CH:19][CH:20]=3)=[N:13][C:12]=2[CH3:21])=[O:10])[CH:2]=1.Br[CH2:23][C:24]1[CH:29]=[CH:28][C:27]([S:30]([CH3:33])(=[O:32])=[O:31])=[CH:26][CH:25]=1>>[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([CH2:7][NH:8][C:9]([C:11]2[S:15][C:14]([C:16]3[CH:20]=[CH:19][N:18]([CH2:23][C:24]4[CH:25]=[CH:26][C:27]([S:30]([CH3:33])(=[O:32])=[O:31])=[CH:28][CH:29]=4)[N:17]=3)=[N:13][C:12]=2[CH3:21])=[O:10])[CH:2]=1

Participants

3

Reactant 2

HCID 27335814-(Methylsulfonyl)benzyl BromideHCID 866455594-methyl-2-(2H-pyrazol-3-yl)-thiazole-5-carboxylic acid (pyridin-3-ylmethyl)-amide

Product 1

HCID 249564922-[1-(4-methanesulfonyl-benzyl)-1H-pyrazol-3-yl]-4-methyl-thiazole-5-carboxylic acid (pyridin-3-ylmethyl)amide

Procedure

The title compound was prepared from 4-methyl-2-(2H-pyrazol-3-yl)-thiazole-5-carboxylic acid (pyridin-3-ylmethyl)-amide and 1-bromomethyl-4-methanesulfonyl-benzene as described in Example 49 and isolated as a white solid (0.058 mg, 45% yield). 1HNMR (400 MHz, CDCl3) δ 8.61 (s, 1H), 8.57 (d, J=4 Hz, 1H), 7.91 (d, J=8 Hz, 2H), 7.70 (d, J=8 Hz, 1H), 7.48 (d, J=2 Hz, 1H), 7.40 (d, J=8 Hz, 2H), 7.26-7.32 (m, 1H), 6.89 (d, J=4 Hz, 1H), 6.03-6.12 (m, 1H), 5.44 (s, 2H), 4.63 (d, J=4 Hz, 2H), 3.03 (s, 3H), 2.75 (s, 3H); MS (M+H)+=468.1; Rt=0.99 min; HRMS (M+H)+=468.12.

Sources & evidence

ORD record
ord-47eae05223654ef5bd42835b12f061f2
Source dataset
uspto-grants-2012_11
Patent number
US08314138B2

Reaction notes

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