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HRID 80182作成日:2026年10月26日

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

https://huagongshe.com/reaction/80182

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物6-AminobenzothiazoleHCID 68288—
反応物Aminoacetaldehyde dimethyl acetalHCID 89728—
反応物TriphosgeneHCID 94429—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物1-Benzothiazol-6-yl-3-(2,2-dimethoxy-ethyl)-ureaHCID 68785445228.8%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号USRE045173E1
出典データセットuspto-grants-2014_09
ORD IDord-fa3dd9ed285e48509a13759cf84a641d
出典メモuspto-grants-2014_09