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HRID 241254作成日:2026年10月25日

[4-(1,3-Thiazol-2-yl)phenyl]methanol → tert-Butyl [tert-butoxycarbonyl(6-{(pyridin-3-ylsulfonyl)[4-(thiazol-2-yl)benzyl]-aminomethyl}pyridin-2-yl)amino]acetate

https://huagongshe.com/reaction/241254

反応式

関与物質

役割名称HCID仕込み量
反応物[4-(1,3-Thiazol-2-yl)phenyl]methanolHCID 24229487—
反応物N-[4-(thiazol-2-yl)benzyl]pyridin-3-ylsulfonamideHCID 66717376—
反応物Tert-butyl (tert-butoxycarbonyl{6-[(pyridin-3-ylsulfonyl)aminomethyl]pyridin-2-yl}amino)acetateHCID 86651773—
反応物Butyl [tert-butoxycarbonyl(6-hydroxymethylpyridin-2-yl)amino]acetateHCID 86651774—
生成物tert-Butyl [tert-butoxycarbonyl(6-{(pyridin-3-ylsulfonyl)[4-(thiazol-2-yl)benzyl]-aminomethyl}pyridin-2-yl)amino]acetateHCID 8665177285%

反応手順

Reaction and post-treatment were carried out in the same manner as in Example 2-(a) except for using tert-butyl(tert-butoxycarbonyl{6-[(pyridin-3-ylsulfonyl)aminomethyl]pyridin-2-yl}amino)acetate (126 mg, 0.263 mmol) obtained in Reference Example 12-(d) in place of N-[4-(thiazol-2-yl)benzyl]pyridin-3-ylsulfonamide, and using 4-(thiazol-2-yl)benzyl alcohol (49.7 mg, 0.260 mmol) obtained in Reference Example 4-(a) in place of text-butyl[tert-butoxycarbonyl(6-hydroxymethylpyridin-2-yl)amino]acetate to afford the title compound (145 mg) as a white foam. (Yield: 85%)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08648097B2
出典データセットuspto-grants-2014_02
ORD IDord-9a579c33ede44053891cc8bc9078e3da
出典メモuspto-grants-2014_02