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HRID 1425242作成日:2026年10月25日

Methyl cis(+/-)-5-(4-{[(benzyloxy)carbonyl]amino}-3-methoxypiperidin-1-yl)-2-methylpyridine-3-carboxylate → Methyl cis(+/-)-5-(4-amino-3-methoxypiperidin-1-yl)-2-methylpyridine-3-carboxylate

https://huagongshe.com/reaction/1425242

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl cis(+/-)-5-(4-{[(benzyloxy)carbonyl]amino}-3-methoxypiperidin-1-yl)-2-methylpyridine-3-carboxylateHCID 86648719—
触媒HCID 178418390HCID 178418390—
生成物Methyl cis(+/-)-5-(4-amino-3-methoxypiperidin-1-yl)-2-methylpyridine-3-carboxylateHCID 8664872174.3%

反応手順

The same operation as in Example (160c) was performed using methyl cis(±)-5-(4-{[(benzyloxy)carbonyl]amino}-3-methoxypiperidin-1-yl)-2-methylpyridine-3-carboxylate obtained in Example (171a) (225 mg) and a 10% palladium-carbon catalyst (250 mg), to obtain 113 mg of the title compound as a yellow oily substance. 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-0bcb8051249e4661a88823027b3a4050
出典メモuspto-grants-2015_01