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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 476569Generated: October 29, 2026

1-Methylpiperazine → HCID 14423122, compound

https://huagongshe.com/reaction/476569

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
ReactantHCID 14098030HCID 14098030—
ProductHCID 14423122HCID 1442312215.8%

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixture of 6-chloro-1-methoxycarbonylmethyl-2-oxo-1,2-dihydrothiazolo[5,4-b]pyridine (2.0 g) and N-methyl-piperazine (1.6 g) was heated at 130° C. for 15 min. After cooling, the mixture was purified on a silica gel column chromatography using a mixture of chloroform 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 chloroform and diethyl ether to give 6-chloro-2-oxo-1-[(4-methyl-1-piperazinyl)carbonylmethyl]-1,2-dihydrothiazolo[5,4-b]pyridine (0.4 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04885297
Source datasetuspto-grants-1989_12
ORD IDord-28b77e37065b41bd9172f852a57dbe5a
Source noteuspto-grants-1989_12