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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21729Generated: October 26, 2026

Sodium Hydroxide → 2,4-Dichloro-7-(6,6-dimethyl-3,5,6,7-tetrahydropyrrolo-[2,1-c][1,2,4]thiadiazol-3-ylidenamino)-6-fluorobenzothiazole

https://huagongshe.com/reaction/21729

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantBromineHCID 24408—
Reactant2-Amino-4,4-dimethylpyrroline hydrochlorideHCID 19933461—
Reactant2,4-Dichloro-6-fluoro-7-isothiocyanatobenzothiazoleHCID 19933464—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product2,4-Dichloro-7-(6,6-dimethyl-3,5,6,7-tetrahydropyrrolo-[2,1-c][1,2,4]thiadiazol-3-ylidenamino)-6-fluorobenzothiazoleHCID 53968206—

Reaction Conditions

Temperature2 °C

Reaction Steps

A solution of 2 g 2,4-dichloro-6-fluoro-7-isothiocyanatobenzothiazole in 10 ml dichloromethane was added, dropwise, at 0° C., to a suspension of 1.1 g 2-amino-4,4-dimethylpyrroline hydrochloride in 20 ml dichloromethane. A solution of 0.3 g sodium hydroxide and 6 ml water was added, dropwise, at 2° C. to this mixture which was stirred for 3 hours, whereby the temperature rose to 20° C. The mixture was cooled to -10° C. and a solution of 1 g bromine in 10 ml dichloromethane was added, dropwise, slowly and the mixture stirred for I hour whereby the temperature rose to 10° C. The solution was washed with water and with dilute caustic soda, dried over magnesium sulfate and concentrated. The residue was recrystallised from diisopropyl ether. Yield: 1.5 g=53% of theory m.p.: 134°-136° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05424443
Source datasetuspto-grants-1995_06
ORD IDord-d804bd441201440e948ae6abc9e51e2d
Source noteuspto-grants-1995_06