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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2383866Generated: October 27, 2026

Ethyl Acetate → 1-Benzothiazol-6-yl-3-(2,2-dimethoxy-ethyl)-urea

https://huagongshe.com/reaction/2383866

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant6-AminobenzothiazoleHCID 68288—
ReactantAminoacetaldehyde dimethyl acetalHCID 89728—
ReactantTriphosgeneHCID 94429—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product1-Benzothiazol-6-yl-3-(2,2-dimethoxy-ethyl)-ureaHCID 68785445228.8%

Reaction Steps

TEA (185 mL, 1.3315 mmol) and triphosgene (138 mg, 0.4660 mmol) were added to a solution of benzothiazol-6-ylamine (200 mg, 1.3315 mmol) in THF (20 mL) at 0° C. The resulting mixture was stirred at room temperature for 3 hours. This was followed by the addition of 2,2-dimethoxy-ethylamine (173 mL, 1.5978 mmol) in THF and TEA (185 mL, 1.3315 mmol) and the stirring was continued for a further 18 hours at room temperature. The reaction was monitored by TLC (50% ethylacetate in hexane). The reaction mixture was concentrated and the concentrate was partitioned between ethylacetate and water. The organic layer was washed with water, brine solution, dried over Na2SO4 and concentrated. Purification by column chromatography on silica gel (100% ethylacetate) afforded 300 mg of 1-Benzothiazol-6-yl-3-(2,2-dimethoxy-ethyl)-urea (80.21% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263635B2
Source datasetuspto-grants-2012_09
ORD IDord-26481b10f50c4eb3960317e1d630d640
Source noteuspto-grants-2012_09