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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1752388Generated: October 29, 2026

Ammonia → 2,6-Dichloropyrimidine-4-carboxamide

https://huagongshe.com/reaction/1752388

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant1,4-DioxaneHCID 31275—
ReactantDiisopropylethylamineHCID 81531—
Reactant2,6-dichloropyrimidine-4-carbonyl ChlorideHCID 11031133—
SolventDiethyl EtherHCID 3283—
Product2,6-Dichloropyrimidine-4-carboxamideHCID 24112841.1%

Reaction Steps

To a solution of 2,6-dichloropyrimidine-4-carbonyl chloride (26.13 g, 123.6 mmol) in Et2O (500 mL) was added a mixture of 0.5M ammonia in dioxane (250 mL, 125 mmol) and iPr2NEt (22 mL, 126 mmol) dropwise over approximately 50 minutes. After stirring overnight the reaction was concentrated in vacuo to a residue and chromatographed over silica gel with 10-50% EtOAc in hexanes. The product fractions were evaporated in vacuo, and the resulting solid residue triturated with 10 mL 10% EtOAc/hexanes and filtered to give 2,6-dichloropyrimidine-4-carboxamide as an orange crystalline solid (9.743 g, 50.74 mmol, 41% yield). LC/MS: m/z=192.2 [M+H]+, 1H NMR (400 MHz, DMSO-d6): 8.40 (1H, br s), 8.16 (1H, br s), 8.10 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09163008B2
Source datasetuspto-grants-2015_10
ORD IDord-ba80fda56709426fb6d2230b453c3d22
Source noteuspto-grants-2015_10