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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2250715Generated: October 26, 2026

4-Methoxy-2-aminobenzothiazole → 1-Benzyl-3-(4-methoxybenzo[d]thiazol-2-yl)urea

https://huagongshe.com/reaction/2250715

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxy-2-aminobenzothiazoleHCID 21622—
ReactantBenzyl isocyanateHCID 76639—
SolventTetrahydrofuranHCID 8028—
Product1-Benzyl-3-(4-methoxybenzo[d]thiazol-2-yl)ureaHCID 22283426—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a stirred solution of 2-amino-4-methoxy-benzothiazole (180 mg, 1 mol) in THF (5 ml) was added benzylisocyanate (166 mg, 1.25 mmol) and the mixture heated to 60° C. for 3 h. After evaporation of the solvent, ether (5 ml) was added and the suspension ultra-sonnicated for 10 min with addition of nHexane (5 ml). This suspension was filtered and washed further with ether/nHexane (1:1) to afford the title compound, after drying under vacuum, as a white solid (220 mg, 70% yield), MS: m/e=313 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07317007B2
Source datasetuspto-grants-2008_01
ORD IDord-b7c8164b8ce34d86ac8a6c4d2939fade
Source noteuspto-grants-2008_01