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HRID 1425017作成日:2026年10月25日

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

https://huagongshe.com/reaction/1425017

反応式

関与物質

役割名称HCID仕込み量
反応物CyclopropanecarboxaldehydeHCID 123114—
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-[(cyclopropylmethyl)amino]piperidin-1-yl)-1,3-benzothiazole-7-carboxylateHCID 8664856193%

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) (37 mg, 0.071 mmol), cyclopropanecarbaldehyde (6.5 μL, 0.087 mmol) and sodium (triacetoxy)borohydride (44 mg, 0.21 mmol), to obtain 35.3 mg of the title compound as a white solid (93%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08927588B2
出典データセットuspto-grants-2015_01
ORD IDord-49d47fb477de4d5880497947f28feeea
出典メモuspto-grants-2015_01