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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2291579Generated: October 31, 2026

Dimethylformamide → HCID 19837972, compound

https://huagongshe.com/reaction/2291579

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantN-HydroxysuccinimideHCID 80170—
ReactantHCID 11010206HCID 11010206—
ProductHCID 19837972HCID 19837972—

Reaction Steps

To an ice-cooled solution of a mixture of 6-chloro-1-carboxymethyl-2-oxo-1,2-dihydrothiazolo[5,4-b]pyridine (3.47 g) and N-hydroxysuccinimide (1.96 g) in N,N-dimethylformamide (20 ml) was gradually added N,N-dicyclohexylcarbodiimide (3.51 g). The mixture was stirred for 1 hour at ambient temperature and dicyclohexylurea that precipitated from the reaction mixture was removed by filtration. To a solution of piperazine (6.11 g) in N,N-dimethylformamide (80 ml) was added dropwise the filtrate for a period of 1.5 hours below 20° c. The final mixture was stirred for 4 hours at ambient temperature, and then filtered. The filtrate was concentrated under reduced pressure below 50° C. and the residue was dissolved in 2N hydrochloric acid. The aqueous solution was washed with chloroform and then adjusted to pH 9 with an aqueous solution of sodium hydrogen carbonate. The turbid solution was extracted with chloroform, and the extract was dried over magnesium sulfate and concentrated under reduced pressure to give a white powder of 6-choro-2-oxo-1-[(1-piperazinyl)carbonylmethyl]-1,2-dihydrothiazolo[5,4 -b]pyridine (3.24 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04797399
Source datasetuspto-grants-1989_01
ORD IDord-091ec2f0ad2445b4ba6b64880afa5eb4
Source noteuspto-grants-1989_01