Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2291580Generated: October 31, 2026

Dimethylformamide → HCID 21278869, compound

https://huagongshe.com/reaction/2291580

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantN-HydroxysuccinimideHCID 80170—
Reactant(2-oxo-1,3-benzothiazol-3(2H)-yl)acetic acidHCID 704583—
ProductHCID 21278869HCID 21278869—

Reaction Steps

To an ice-cooled solution of 2-oxo-3-benzothiazolineacetic acid [J. Prakt. Chem. 27 (3-4), 220-4 (1965); 8.1 g] and N-hydroxysuccinimide (5.4 g) in N,N-dimethylformamide (50 ml) was gradually added N,N-dicyclohexylcarbodiimide (9.6 g), and the mixture was stirred for an hour at ambient temperature. The dicyclohexylurea that precipitated from the reaction mixture was filtered off. To a stirred solution of piperazine (16.7 g) in N,N-dimethylformamide (200 ml) was added dropwise the filtrate for a period of 40 minutes below 20° C. The final mixture was stirred for 3.5 hours at ambient temperature and then filtered. The filtrate was concentrated under reduced pressure. The residue was dissolved in 2N hydrochloric acid and the solution was washed with chloroform. The aqueous layer was adjusted to pH 9 with an aqueous solution of sodium hydrogen carbonate, and the turbid solution was extracted with chloroform (80 ml×3). The extracts were combined and dried over magnesium sulfate. After evaporation of the solvent, 3-[(1-piperazinyl)carbonylmethyl]-2-benzothiazolinone (9.50 g) was obtained as white powders.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04797399
Source datasetuspto-grants-1989_01
ORD IDord-037f6615111f4c0ea93526a7a21f6551
Source noteuspto-grants-1989_01