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HRID 218551作成日:2026年10月27日

6-(Propan-2-yl)pyridin-3-amine → 5-benzyloxy-8-fluoro-N-(6-isopropylpyridin-3-yl)-1,2,3,4-tetrahydronaphthalene-1-carboxamide

https://huagongshe.com/reaction/218551

反応式

関与物質

役割名称HCID仕込み量
反応物6-(Propan-2-yl)pyridin-3-amineHCID 17854288—
反応物5-Benzyloxy-8-fluoro-1,2,3,4-tetrahydronaphthalene-1-carboxylic acidHCID 17854540—
生成物5-benzyloxy-8-fluoro-N-(6-isopropylpyridin-3-yl)-1,2,3,4-tetrahydronaphthalene-1-carboxamideHCID 1785416088.6%

反応手順

By the reaction and treatment in the same manner as in Preparation Example 11 using 5-benzyloxy-8-fluoro-1,2,3,4-tetrahydronaphthalene-1-carboxylic acid (2.30 g) and 5-amino-2-isopropylpyridine (1.04 g) as starting materials, 5-benzyloxy-8-fluoro-N-(6-isopropylpyridin-3-yl)-1,2,3,4-tetrahydronaphthalene-1-carboxamide (2.83 g) was obtained. melting point: 184.0° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08198454B2
出典データセットuspto-grants-2012_06
ORD IDord-be84fb88189349caa9992b3dcbf58368
出典メモuspto-grants-2012_06