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HRID 711496作成日:2026年10月27日

Methyl 2-(3-(tert-butoxycarbonylamino)prop-1-ynyl)-4-methyl-6-(m-tolylamino)pyrimidine-5-carboxylate → Methyl 2-(3-(tert-butoxycarbonylamino)propyl)-4-methyl-6-(m-tolylamino)pyrimidine-5-carboxylate

https://huagongshe.com/reaction/711496

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl 2-(3-(tert-butoxycarbonylamino)prop-1-ynyl)-4-methyl-6-(m-tolylamino)pyrimidine-5-carboxylateHCID 58317513—
触媒PalladiumHCID 23938—
溶媒EthanolHCID 702—
生成物Methyl 2-(3-(tert-butoxycarbonylamino)propyl)-4-methyl-6-(m-tolylamino)pyrimidine-5-carboxylateHCID 58317633—

反応手順

Methyl 2-(3-(tert-butoxycarbonylamino)prop-1-ynyl)-4-methyl-6-(m-tolylamino)pyrimidine-5-carboxylate (0.190 g, 0.463 mmol) was dissolved in EtOH (4 mL). To this solution was added palladium on carbon (0.049 g, 0.046 mmol) and the resulting mixture was stirred overnight at RT under H2 atmosphere. The mixture was filtered through a pad of Celite, and the filtrate was evaporated to give the title compound as a brown oil, which was used in next step without further purification. [M+H] calc'd for C22H30N4O4, 415. found, 415.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09181255B2
出典データセットuspto-grants-2015_11
ORD IDord-abd61ac52e3a442ab95f90203e68d37c
出典メモuspto-grants-2015_11