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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2106784Generated: October 30, 2026

Acetyl chloride → HCID 131716404, compound

https://huagongshe.com/reaction/2106784

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
ReactantSodium CarbonateHCID 10340—
ReactantHCID 131716406HCID 131716406—
SolventDichloromethaneHCID 6344—
ProductHCID 131716404HCID 13171640465.4%

Reaction Steps

In 10 ml of dichloromethane were dissolved 1.00 g of dl-5-chloro-6-ethyl-4-(6-hydroxyhexyl)aminopyrimidine and 0.40 g of acetyl chloride, and under stirring, 0.50 g of triethylamine was added to the solution and the mixture was stirred at room temperature for 30 minutes. After completion of the reaction, the reaction mixture was neutralized with an aqueous sodium carbonate solution and extracted with dichloromethane. After the organic layer was dried over anhydrous sodium sulfate, the solvent was removed under reduced pressure. The resulting oily product was isolated through a column chromatography (Wako gel C-200, trade name, eluent; toluene:ethyl acetate=4:1) to give 0.70 g of the title compound as pale yellow oily product. nD19.6 1.5228.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04931455
Source datasetuspto-grants-1990_06
ORD IDord-3080e7f067384e8f828ca7e67a4802da
Source noteuspto-grants-1990_06