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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1758743Generated: October 31, 2026

Cyanamide → HCID 178512624, compound

https://huagongshe.com/reaction/1758743

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanamideHCID 9864—
ReactantSodium CarbonateHCID 10340—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 178478805HCID 178478805—
SolventWaterHCID 962—
ProductHCID 178512624HCID 17851262447.8%

Reaction Steps

A mixture of 43 g (0.15 mol) of 2-amino-1-(2-guanidino-4-thiazolyl)ethanone dihydrochloride, 12.6 g (0.30 mol) of cyanamide, and 400 ml of water was brought to pH 4.5 by the dropwise addition of 20% sodium hydroxide solution. The mixture was heated at 50°-60° for 16 hours. The mixture was cooled, made basic with aqueous sodium carbonate solution and the resulting precipitate was collected by filtration, then washed successively with cold water, acetone, and ether. The dried solid was purified by dissolving in a minimum of dimethylformamide, then slowly adding ethyl acetate. Initially tarry material precipitated which was removed by decanting. Further addition of ethyl acetate afforded 16 g of a tan solid. This was again purified by the dimethylformamide-ethyl acetate procedure described above to give 12 g of a tan solid. Recrystallization of this material from methanol/water afforded analytically pure title compound as tan needles, mp 267° (dec). Calcd. for C7H9N7S: C, 37.66; H, 4.06; N, 43.91; S, 14.36; found: C, 37.81; H, 4.31; N, 43.76.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04374843
Source datasetuspto-grants-1983_02
ORD IDord-2c108bc51ec4426e98e33c6c3901a404
Source noteuspto-grants-1983_02