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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 447023Generated: October 30, 2026

Ammonia → 1-(7-Amino-5-pyridin-3-yl-benzothiazol-2-yl)-3-ethyl-urea

https://huagongshe.com/reaction/447023

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantStannous ChlorideHCID 24479—
Reactant1-Ethyl-3-(7-nitro-5-pyridin-3-yl-benzothiazol-2-yl)-ureaHCID 57813624—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product1-(7-Amino-5-pyridin-3-yl-benzothiazol-2-yl)-3-ethyl-ureaHCID 57813571162.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

A stirred suspension of 1-Ethyl-3-(7-nitro-5-pyridin-3-yl-benzothiazol-2-yl)-urea (25 mg, 0.0728 mmol) in ethanol (0.5 ml) and concentrated hydrochloric acid (0.5 ml) was treated with tin (II) chloride (69 mg, 0.364 mmol) and heated at 80° C. for 5 h. After cooling to ambient temperature, the mixture was diluted with water (50 ml) and made alkaline (pH 11) by the addition of concentrated ammonia. The 1-(7-Amino-5-pyridin-3-yl-benzothiazol-2-yl)-3-ethyl-urea was extracted with ethyl acetate (3×50 ml) which was dried (MgSO4) and the solvent removed in vacuo to give an off-white solid (37 mg) which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481544B2
Source datasetuspto-grants-2013_07
ORD IDord-f9acfed292ea48f3992a1898fdae4abd
Source noteuspto-grants-2013_07