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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 476568Generated: October 30, 2026

1-(2-Hydroxyethyl)piperazine → HCID 14423121, compound

https://huagongshe.com/reaction/476568

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Hydroxyethyl)piperazineHCID 7677—
ReactantHCID 14098030HCID 14098030—
ProductHCID 14423121HCID 1442312140%

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixture of 6-chloro-1-methoxycarbonylmethyl-2-oxo-1,2-dihydrothiazolo[5,4-b]pyridine (10.32 g) and N-(2-hydroxyethyl)piperazine (10.4 g) was heated at 130° C. for 15 min. After cooling, the reaction mixture was poured into an ice-water. The precipitates obtained were extracted with chloroform. The chloroform layer was dried over magnesium sulfate, and evaporated to give crude material. The crude material was purified on a silica gel column chromatography using a mixture of methylene chloride and methanol (10:1). The desired fractions containing the objective compound were collected and evaporated. The crude crystals obtained were recrystallized from a mixture of methanol and diethyl ether to give 6-chloro-2-oxo-1-{[4-(2-hydroxyethyl)-1-piperazinyl]carbonylmethyl}-1,2-dihydrothiazolo[5,4-b]pyridine (5.70 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04885297
Source datasetuspto-grants-1989_12
ORD IDord-84cac937ae724fc8944d076492b513b9
Source noteuspto-grants-1989_12