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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1035677Generated: October 30, 2026

2-Aminothiazole → HCID 25072940, compound

https://huagongshe.com/reaction/1035677

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 25069442HCID 25069442—
SolventDichloromethaneHCID 6344—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 25072940HCID 2507294013%

Reaction Steps

To 3-(2-hydroxy-6-(3-hydroxyphenyl)naphthalene-1-yl)benzoic acid (79 mg, 0.22 mmol, 1 eq), which is dissolved under a nitrogen atmosphere in 2 ml of dry DME, thionyl chloride (100 μl) is added, and the mixture is stirred at RT for 2 h. After the excess thionyl chloride has been removed in vacuum on a rotary evaporator, the residue is dissolved in dry DME and added dropwise to a suspension of 2-aminothiazole (22.2 mg, 0.22 mmol, 1 eq) in dry dichloromethane cooled at 0° C. The reaction mixture is stirred at RT over night, followed by removing the solvent on a rotary evaporator. Purification of the raw product by column chromatography with dichloromethane/methanol 95/5 as the eluent yielded the desired compound in a yield of 13%, 13 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546392B2
Source datasetuspto-grants-2013_10
ORD IDord-f97beec9a8534dda8e339b6fce37620b
Source noteuspto-grants-2013_10