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HRID 9133作成日:2026年10月24日

1-(6-Phenylacetylenyl-2-benzothiazolyl)-3-ethylurea → 1-(6-(2(Z)-Phenylvinyl)-2-benzothiazolyl)-3-ethylurea

https://huagongshe.com/ja/reaction/9133

反応式

関与物質

役割名称HCID仕込み量
反応物1-(6-Phenylacetylenyl-2-benzothiazolyl)-3-ethylureaHCID 21985545—
触媒Lindlars catalystHCID 131709914—
溶媒EthanolHCID 702—
生成物1-(6-(2(Z)-Phenylvinyl)-2-benzothiazolyl)-3-ethylureaHCID 8658897341%

反応手順

A suspension of 1-(6-phenylacetylenyl-2-benzothiazolyl)-3-ethylurea (0.032 g, 83% purity by weight, 0.083 mmol) and Lindlar catalyst (0.030 g, 5% weight purity, 0.012 mmol, 0.15 eq) in 2 mL ethanol was purged with nitrogen gas, followed by bubbling of hydrogen gas. It was stirred under hydrogen atmosphere for about 36 hours. The mixture was taken up in 10 mL MeOH, filtered, concentrated, and purified by preparative TLC to give 0.011 g (41%) of the desired compound. LC/MS 324 (M+1); LC retention time 2.84 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07091227B2
出典データセットuspto-grants-2006_08
ORD IDord-b034843c1eae49b58ee346d1b1960c87
出典メモuspto-grants-2006_08