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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 364187Generated: October 31, 2026

3-(2-Chloroethyl)-1,3-oxazolidin-2-one → HCID 13689044, compound

https://huagongshe.com/reaction/364187

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(2-Chloroethyl)-1,3-oxazolidin-2-oneHCID 75633—
ReactantHCID 13689033HCID 13689033—
SolventChloroformHCID 6212—
ProductHCID 13689044HCID 13689044—

Reaction Conditions

Temperature150 °C

Reaction Steps

A mixture of 5.8 g 0.017 mol) of 5-amino-N,N-diethyl-2H[1]benzothiopyrano[4,3,2-cd]indazole-2-ethanamine and 5.1 g (0.034 mol) of 3-(2-chloroethyl)-2-oxazolidinone was stirred at 150° C. for two hours, dissolved in 100 ml of CHCl3 and washed twice with 2N NaOH. The solution was dried (MgSO4) and concentrated in vacuo to dryness. The residue was flash chromatographed over silica gel, eluting with a CHCl3 /MeOH (4/1) mixture. The appropriate fractions were combined and concentrated to dryness in vacuo. The residue was treated with 20 ml of acetone and the resulting suspension was treated with 150 ml of Et2O. The resulting precipitate was collected and dried to give 4.9 g of product, mp 90°-94° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04604390
Source datasetuspto-grants-1986_08
ORD IDord-59084415c0ba4959b94975e188c07e95
Source noteuspto-grants-1986_08