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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 650636Generated: October 30, 2026

Dichloromethane → 2-Methylsulfanyl-4-o-tolyl-pyrimidine-5-carboxylic acid (3,5-dimethyl-benzyl)-methyl-amide

https://huagongshe.com/reaction/650636

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant2-Methylsulfanyl-4-o-tolyl-pyrimidine-5-carboxylic acidHCID 21712434—
Product2-Methylsulfanyl-4-o-tolyl-pyrimidine-5-carboxylic acid (3,5-dimethyl-benzyl)-methyl-amideHCID 5378848882%

Reaction Steps

To a solution of 2.60 g (9.99 mmol) 2-methylsulfanyl-4-o-tolyl-pyrimidine-5-carboxylic acid in 70 ml CH2Cl2 2.78 ml (19.98 mmol) triethylamine, 1.34 g (9.99 mmol) 1-hydroxybenzotriazole and 1.91 g (9.99 mmol) N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride 1.78 g (11.99 mmol) (3,5-dimethoxy-benzyl)-methyl-amine were added. The reaction mixture was stirred for 16 hrs. The reaction mixture was diluted with 100 ml CH2Cl2, washed with 100 ml 0.5N HCl and 100 ml H2O. The aqueous layers were backextracted with 100 ml CH2Cl2. The combined organic layers were dried (MgSO4), filtered and evaporated. The residue was purified by chromatography (SiO2, CH2Cl2/MeOH 40:1) to give 3.20 g (82%) 2-methylsulfanyl-4-o-tolyl-pyrimidine-5-carboxylic acid (3,5-dimethyl-benzyl)-methyl-amide as a pale yellow oil, MS (EI): 391 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06274588B1
Source datasetuspto-grants-2001_08
ORD IDord-f7171ddf1ff44aaf84d1d91055a8d721
Source noteuspto-grants-2001_08