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HRID 908348作成日:2026年10月26日

Potassium Carbonate → 8-(3-Sulfamoyl-phenylamino)-4,5-dihydro-thiazolo[4,5-h]quinazoline-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/908348

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物Ethyl 7-oxo-4,5,6,7-tetrahydro-1,3-benzothiazole-2-carboxylateHCID 14955933—
反応物N,N-dimethylformamide N,N-dimethylacetamideHCID 22628260—
反応物HCID 178479386HCID 178479386—
溶媒WaterHCID 962—
生成物8-(3-Sulfamoyl-phenylamino)-4,5-dihydro-thiazolo[4,5-h]quinazoline-2-carboxylic acid ethyl esterHCID 5926282824%

反応条件

温度120 °C

反応手順

To 7-oxo-4,5,6,7-tetrahydro-benzothiazole-2-carboxylic acid ethyl ester (0.1128 g, 0.50 mmol) was added DMF/DMA solution (3 mL) and the mixture was refluxed under nitrogen for 1 hour. The reaction mixture was concentrated in vacuo and the resulting crude product (6-dimethylaminomethylene-7-oxo-4,5,6,7-tetrahydro-benzothiazole-2-carboxylic acid ethyl ester) was taken through to the next step without further purification. The above was dissolved in anhydrous DMA (3 mL) and treated with 3-guanidino-benzenesulfonamide hydrogen chloride (128 mg, 0.51 mmol) and powdered potassium carbonate (35 mg, 0.26 mmol). The mixture was heated to 120° C. with vigorous stirring for 12 hours. The mixture was cooled down to room temperature, and diluted with water. The resulting solid was filtered, rinsed with more water, a little bit of iPrOH and Et2O. The crude solid was purified by silica gel to give the title compound as a brown solid in 24% yield (52 mg). MS (ES+) 432, (ES−) 430. δH (d6 DMSO) 1.36 (3H, t), 3.05 (2H, t), 3.17 (2H, t), 4.42 (2H, q), 7.33 (2H, s), 7.41 (1H, d), 7.50 (1H, t), 7.89 (1H, d), 8.43 (1H, t), 8.52 (1H, s), 10.04 (1H, s).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08017619B2
出典データセットuspto-grants-2011_09
ORD IDord-39aae3cc59164085bd62a481e934cd97
出典メモuspto-grants-2011_09