Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1035773Generated: October 25, 2026

Cyclopropanecarbonyl chloride → 2-[(Cyclopropylcarbonyl)amino]-1,3-benzothiazol-6-yl thiocyanate

https://huagongshe.com/reaction/1035773

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopropanecarbonyl chlorideHCID 77637—
Reactant2-Amino-6-thiocyanato-1,3-benzothiazoleHCID 81600—
SolventPyridineHCID 1049—
Product2-[(Cyclopropylcarbonyl)amino]-1,3-benzothiazol-6-yl thiocyanateHCID 86647894—

Reaction Steps

The 2-[(cyclopropylcarbonyl)amino]-1,3-benzothiazol-6-yl thiocyanate was prepared in a manner similar to the method described in Example 18b, but using 2 g of commercial 2-amino-6-thiocyanatobenzothiazole and 1.21 g of cyclopropanecarboxylic acid chloride in 20 cm3 of pyridine after reaction for 5 h at 20° C. 2.65 g of 2-[(cyclopropylcarbonyl)amino]-1,3-benzothiazol-6-yl thiocycanate are thus obtained in the form of a yellow powder, the characteristics of which are as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546393B2
Source datasetuspto-grants-2013_10
ORD IDord-ed4e41f905554695908b439b14297db5
Source noteuspto-grants-2013_10