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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1879153Generated: October 26, 2026

Dimethylformamide → 2-(6-Dimethylamino-pyrazin-2-yl)-4-methyl-thiazole-5-carboxylic acid benzylamide

https://huagongshe.com/reaction/1879153

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant2-(6-Iodo-pyrazin-2-yl)-4-methyl-thiazole-5-carboxylic acid benzylamideHCID 73213269—
SolventDichloromethaneHCID 6344—
Product2-(6-Dimethylamino-pyrazin-2-yl)-4-methyl-thiazole-5-carboxylic acid benzylamideHCID 2495470380%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a sealed tube was added 2-(6-iodo-pyrazin-2-yl)-4-methyl-thiazole-5-carboxylic acid benzylamide (See Example 2, 50 mg, 0.11 mmol, 1.0 equiv) and dimethyl formamide (1 mL). The reaction mixture was stirred at 100° C. After 18 hr, the reaction mixture was cooled to room temperature and diluted with dichloromethane washed with saturated NaHCO3, brine, dried (Na2SO4), filtered, and concentrated in vacuo. The crude product was purified by preparative HPLC (acetonitrile/water, 0.1% trifluoroacetic acid) to afford 2-(6-dimethylamino-pyrazin-2-yl)-4-methyl-thiazole-5-carboxylic acid benzylamide (32 mg, 80%). 1H NMR (400 MHz, CD2Cl2) δ 8.51 (s, 1H), 8.06 (s, 1H), 7.29-7.36 (m, 5H), 6.21 (bs, 1H), 4.59 (d, J=8.0 Hz, 2H), 3.17 (s, 6H), 2.71 (s, 3H); HRMS (M+H)+=354.13.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314138B2
Source datasetuspto-grants-2012_11
ORD IDord-a9fb413e86744b5989d1387a7ce940d3
Source noteuspto-grants-2012_11