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HRID 353737作成日:2026年10月25日

Cyanamide → [4-Amino-2-[[4-(4-methyl-1-piperazinyl)phenyl]amino]-5-thiazolyl](2,3-dihydro-1,4-benzodioxin-6-yl)methanone

https://huagongshe.com/reaction/353737

反応式

関与物質

役割名称HCID仕込み量
反応物CyanamideHCID 9864—
反応物2-Bromo-1-(2,3-dihydro-1,4-benzodioxin-6-yl)ethan-1-oneHCID 2776171—
反応物1-(4-Isothiocyanatophenyl)-4-methylpiperazineHCID 13718397—
反応物Potassium tert-butoxideHCID 23665647—
溶媒AcetonitrileHCID 6342—
溶媒tert-ButanolHCID 6386—
生成物[4-Amino-2-[[4-(4-methyl-1-piperazinyl)phenyl]amino]-5-thiazolyl](2,3-dihydro-1,4-benzodioxin-6-yl)methanoneHCID 991165266%

反応手順

tert-Butanol (4 mL) and then 1-(4-isothiocyanatophenyl)-4-methyl piperazine (of Example 1; 219 mg, 1 mmol) were added to a solution of cyanamide (44 mg, 1.05 mmol) (Aldrich) in acetonitrile (5 mL). Potassium t-butoxide (1 M in tert-butanol; 1 mL, 1 mmol) was added and the solution was stirred for 30 min. 2-Bromo-1-(2,3-dihydro-1,4-benzodioxin-6-yl)ethanone (257 mg, 1 mmol) (Maybridge Chemical Company Ltd.) was added, and the solution was stirred at room temperature for 3 days. The yellow solid was filtered off and washed with cold acetonitrile and then ether to give [4-amino-2-[[4-(4-methyl-1-piperazinyl)phenyl]amino]-5-thiazolyl](2,3-dihydro-1,4-benzodioxin-6-yl)methanone (280 mg, 66%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06756374B2
出典データセットuspto-grants-2004_06
ORD IDord-ba95a5db59124a359fccdbe0ed662338
出典メモuspto-grants-2004_06