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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1980583Generated: October 30, 2026

Cyanamide → HCID 178512624, compound

https://huagongshe.com/reaction/1980583

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 numberUS04510313
Source datasetuspto-grants-1985_04
ORD IDord-ddd94f2fd1204e849fa53f6dee48fc0e
Source noteuspto-grants-1985_04