Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 236313Generated: October 29, 2026

Dichloromethane → HCID 178512708, compound

https://huagongshe.com/reaction/236313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantSodium HydroxideHCID 14798—
Reactant2,2'-Thiobis(1H-isoindole-1,3(2H)-dione)HCID 82196—
ReactantHCID 178478604HCID 178478604—
SolventTriethylamineHCID 8471—
ProductHCID 178512708HCID 17851270854%

Reaction Steps

A mixture of crude N-{2-[(2-guanidinothiazol-4-yl)methylthio]ethyl}ethanediimidamide trihydrochloride (5.65 g, 13.7 mmoles) [prepared in Step A], 50 ml of CH2Cl2 and 5.7 ml of triethylamine was treated with N,N'-thiobisphthalimide (DMF solvate) (5.44 g; 13.7 mmoles) and stirred for one hour to give a thick suspension. The mixture was treated with 40 ml of 2N NaOH and the solvents were decanted from the gum-like material which had separated. The gum was washed with 40 ml of 2N NaOH, water, and then dissolved in methanol and concentrated to give 3.0 g of crude product. The product was purified by flash chromatography on 90 g of silica gel (230-400 mesh) using ethyl acetate-methanol (97:3) as the eluent to give 2.44 g (54%) of the title compound. Treatment of the product in 35 ml of acetone with one equivalent of cyclohexylsulfamic acid gave the salt which was then recrystallized from 95 % aqueous ethanol to give the title compound as its cyclohexylsulfamate salt, mp. 171°-173.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04644006
Source datasetuspto-grants-1987_02
ORD IDord-9271a862ddf648679bd9597e71b2d674
Source noteuspto-grants-1987_02