Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1715234Generated: November 4, 2026

HCID 178523937, compound → HCID 178514162, compound

https://huagongshe.com/reaction/1715234

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178523937HCID 178523937—
SolventSodium HydroxideHCID 14798—
ProductHCID 178514162HCID 178514162—

Reaction Steps

A solution of N-[(1H-pyrazol-3-ylamino)carbonothioyl]benzamide (22 g, 0.089 mol) in 10% NaOH solution (200 ml) is stirred at 80° C. for 45 min. The reaction mixture is cooled down to rt and the solvents are removed under vacuum. The residue is acidified with 2M HCl to pH=1 and then basified with ammonium hydroxide. The product is extracted with dichloromethane (4×100 ml). The combined extracts are dried and evaporated. The solid residue is purified by flash chromatography using chloroform/methanol (9/1) as eluent. N-1H-Pyrazol-3-ylthiourea is isolated as a solid (9 g; 75%). 1H NMR (DMSO-d6, 300 MHz): δ 5.88 (br s, 1H), 7.64 (s, 1H), 8.44 (br s, 1H), 9.02 (br s, 1H), 10.30 (br s, 1H), 12.47 (br s, 1H). HPLC (Method B), Rt: 3.88 min (purity: 99.4%). TLC: Chloroform/methanol (9/1): Rf−0.2. Mp: 130-132° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07799814B2
Source datasetuspto-grants-2010_09
ORD IDord-600dcb76dd56407c87453aa34da22f95
Source noteuspto-grants-2010_09