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HRID 1425263作成日:2026年10月27日

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

https://huagongshe.com/reaction/1425263

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)-4-fluorobenzoateHCID 86648744—
触媒HCID 178418390HCID 178418390—
生成物Methyl cis(+/-)-3-(4-amino-3-methoxypiperidin-1-yl)-4-fluorobenzoateHCID 8664874626.6%

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)-4-fluorobenzoate obtained in Example (181a) (101 mg, 0.24 mmol) and a 10% palladium-carbon catalyst (100 mg), to obtain 18 mg of the title compound as a colorless oily substance (26%). 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US08927588B2
出典データセットuspto-grants-2015_01
ORD IDord-2b1d63cc4f354e2ab8c2aa25595ec4ce
出典メモuspto-grants-2015_01