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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598204Generated: November 1, 2026

Dimethylformamide → HCID 178457774, compound

https://huagongshe.com/reaction/598204

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantCyanoacetic acidHCID 9740—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 178456731HCID 178456731—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductHCID 178457774HCID 178457774—

Reaction Conditions

Temperature0 °C

Reaction Steps

Cyanoacetic acid (1.63 g, 19.17 mmol) was suspended in anhydrous dichloromethane (40 ml). A catalytic amount of N,N-dimethylformamide (0.1 ml) was added and the mixture cooled to 0° C. under an atmosphere of Argon. After 20 minutes stirring at 0° C., oxalyl chloride (1.67 ml, 19.17 mmol) was slowly added to the reaction mixture, which was then allowed to warm to ambient temperature. This mixture was added slowly, after stirring 1 hour, to a 1 M solution of 6-isopropylamino-1,3-benzothiazole-2-thiol (2.16 g, 9.57 mmol) in anhydrous pyridine. After 2 hours the reaction mixture was concentrated in vacuo and partitioned between ethyl acetate and 1 M aqueous citric acid. The resulting precipitate was collected by filtration, combined with the organic extract and concentrated in vacuo. The residue was triturated with diethyl ether to yield 2.32 g (83%). 1H NMR (DMSO-d6) δ=0.98 (m, 6H), 3.43 (s, 2H), 4.75 (sep, 1H), 7.27 (d, 1H), 7.35 (d, 1H), 7.63 (s, 1H), 13.94 (s, 1H); ESIMS: m/z 290 (M-H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897615B2
Source datasetuspto-grants-2011_03
ORD IDord-97dc467331a1498899e74ec25599df63
Source noteuspto-grants-2011_03