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HRID 30138作成日:2026年10月23日

Ethyl 4-amino-1-piperidinecarboxylate → 4-[6-Amino-5-(2,3-difluoro-6-methoxy-benzoyl)-pyridin-2-ylamino]-piperidine-1-carboxylic acid ethyl ester

https://huagongshe.com/ja/reaction/30138

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl 4-amino-1-piperidinecarboxylateHCID 100867—
反応物(2-Amino-6-chloro-pyridin-3-yl)-(2,3-difluoro-6-methoxy-phenyl)-methanoneHCID 58590826—
生成物4-[6-Amino-5-(2,3-difluoro-6-methoxy-benzoyl)-pyridin-2-ylamino]-piperidine-1-carboxylic acid ethyl esterHCID 11618923—

反応手順

The title compound was prepared from (2-Amino-6-chloro-pyridin-3-yl)-(2,3-difluoro-6-methoxy-phenyl)-methanone (Example 39) and ethyl4-amino-1-piperidine carboxylate (Aldrich 96%) using the procedure described in Step B. Example 6. HRMS, observed: 435.1841, Calcd for (M+H)+: 435.1839.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07423051B2
出典データセットuspto-grants-2008_09
ORD IDord-5c3315121bdc4bc1aad92080981404d0
出典メモuspto-grants-2008_09