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HRID 43759作成日:2026年10月26日

Methyl cis(+/-)-3-(4-{[(benzyloxy)carbonyl]amino}-3-methoxypiperidin-1-yl)benzoate → Methyl cis(+/-)-3-(4-amino-3-methoxypiperidin-1-yl)benzoate

https://huagongshe.com/reaction/43759

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl cis(+/-)-3-(4-{[(benzyloxy)carbonyl]amino}-3-methoxypiperidin-1-yl)benzoateHCID 86648495—
触媒HCID 178418390HCID 178418390—
生成物Methyl cis(+/-)-3-(4-amino-3-methoxypiperidin-1-yl)benzoateHCID 8664870887.5%

反応手順

The same operation as in Example (160c) was performed using methyl cis(±)-3-(4-{[(benzyloxy)carbonyl]amino}-3-methoxypiperidin-1-yl)benzoate obtained in Example (42a) (180 mg) and a 10% palladium-carbon catalyst (150 mg), to obtain 104.5 mg of the title compound as a white solid. The resulting compound was used for the next reaction without purification.

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-e4d7c9fea97e43ada9361d3a3512a57a
出典メモuspto-grants-2013_09