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HRID 515954作成日:2026年10月25日

Selenium Dioxide → HCID 86654702、化合物

https://huagongshe.com/reaction/515954

反応式

関与物質

役割名称HCID仕込み量
反応物Selenium DioxideHCID 24007—
反応物2,4-DimethoxybenzylamineHCID 597250—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物Methyl 2-((1R,2S)-2-(tert-butoxycarbonylamino)cyclohexylamino)-4-methyl-6-(m-tolylamino)pyrimidine-5-carboxylateHCID 67238015—
溶媒MethanolHCID 887—
溶媒1,4-DioxaneHCID 31275—
生成物HCID 86654702HCID 8665470237%

反応条件

温度100 °C

反応手順

A mixture of methyl 2-((1R,2S)-2-(tert-butoxycarbonylamino)cyclohexylamino)-4-methyl-6-(m-tolylamino)pyrimidine-5-carboxylate (500 mg, 1.065 mmol) and selenium dioxide (236 mg, 2.130 mmol) in dioxane (10 mL) was heated at 100° C. for 24 h. The solution was subsequently cooled and filtered. The filtrate was concentrated under reduced pressure and dried to give a brown foam (534 mg; dihydroxyl form was observed via mass spectroscopy), which was used directly in the next step without further purification. A mixture of the unpurified intermediate (534 mg, 1.065 mmol) and (2,4-dimethoxyphenyl)methanamine (0.160 mL, 1.065 mmol) in MeOH (10 mL) was stirred at RT for 10 min, after which sodium cyanoborohydride (100 mg, 1.597 mmol) was added, and the reaction mixture was stirred at RT for 20 h. The reaction mixture was warmed to 50° C. and stirred for an additional 2 h to complete the reaction. The mixture was cooled to RT and the solid filtered and washed with MeOH to give the title compound as a pinkish solid (237 mg, 37%). [M+H] calc'd for C33H42N6O5, 603; found, 603.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09108970B2
出典データセットuspto-grants-2015_08
ORD IDord-529a144e69b14a0abcce5800c386e0ea
出典メモuspto-grants-2015_08