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HRID 43549作成日:2026年10月23日

3-Methylbutanal → Ethyl cis(+/-)-2-(4-{[(4-chloro-5-ethyl-1H-imidazol-2-yl)carbonyl]amino}-3-[(3-methylbutyl)amino]piperidin-1-yl)-1,3-benzothiazole-7-carboxylate

https://huagongshe.com/ja/reaction/43549

反応式

関与物質

役割名称HCID仕込み量
反応物3-MethylbutanalHCID 11552—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物Ethyl cis(+/-)-2-(3-amino-4-{[(4-chloro-5-ethyl-1H-imidazol-2-yl)carbonyl]amino}piperidin-1-yl)-1,3-benzothiazole-7-carboxylateHCID 86648558—
生成物Ethyl cis(+/-)-2-(4-{[(4-chloro-5-ethyl-1H-imidazol-2-yl)carbonyl]amino}-3-[(3-methylbutyl)amino]piperidin-1-yl)-1,3-benzothiazole-7-carboxylateHCID 86648566—

反応手順

The same operation as in Example (77d) was performed using ethyl cis(±)-2-(3-amino-4-{[(4-chloro-5-ethyl-1H-imidazol-2-yl)carbonyl]amino}piperidin-1-yl)-1,3-benzothiazole-7-carboxylate obtained by the method described in Example (81e) (30 mg, 0.063 mmol), 3-methylbutanal (10.8 μL, 0.010 mmol) and sodium (triacetoxy)borohydride (87 mg, 0.41 mmol), to obtain 34.2 mg of the title compound as a colorless oily substance (99%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08536197B2
出典データセットuspto-grants-2013_09
ORD IDord-0d9e86a94c6542f787f5b32b40f531bc
出典メモuspto-grants-2013_09