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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 68298Generated: October 25, 2026

1,2-Dichloroethane → 2-(Methylthio)-6-phenylpyrimidine-4-carboxamide

https://huagongshe.com/reaction/68298

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant4-MethylmorpholineHCID 7972—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant2-(Methylthio)-6-phenylpyrimidine-4-carboxylic acidHCID 39349202—
SolventDimethylformamideHCID 6228—
Product2-(Methylthio)-6-phenylpyrimidine-4-carboxamideHCID 5887276194.1%

Reaction Steps

N-Methylmorpholine (2.31 mL, 21 mmol) was added dropwise by syringe to a mixture of 2-methylsulfanyl-6-phenylpyrimidine-4-carboxylic acid (3.45 g, 14 mmol), ammonium chloride (4.27 g, 80 mmol), HOBt (2.84 g, 21 mmol), and EDC (4.0 g, 21 mmol) in DMF (40 mL) at room temperature. The reaction solution was stirred at room temperature for 3 h before the DMF was removed by rotary evaporation. Column chromatography (SiO2, DCM/EtOAc 5:1) afforded 3.23 g of 2-(methylthio)-6-phenylpyrimidine-4-carboxamide as a white solid. 1H NMR (DMSO-d6, 300 MHz) δ 8.25 (m, 2H), 8.13 (s, 1H), 7.59 (m, 3H), 2.62 (s, 3H). HPLC ret. time 2.71 min, 10-100% CH3CN, 5 min gradient. ESI-MS m/z 246.1 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822451B2
Source datasetuspto-grants-2014_09
ORD IDord-7f173a098f5a4026aa5fcce250a12d7a
Source noteuspto-grants-2014_09