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HRID 2226014作成日:2026年10月23日

Tri-o-tolylphosphine → HCID 178418607、化合物

https://huagongshe.com/ja/reaction/2226014

反応式

関与物質

役割名称HCID仕込み量
反応物Tri-o-tolylphosphineHCID 80271—
反応物diethyl (2S)-2-[(4-iodobenzoyl)amino]pentanedioateHCID 1885228—
反応物HCID 178418674HCID 178418674—
触媒palladium(II) acetateHCID 167845—
溶媒AcetonitrileHCID 6342—
溶媒TriethylamineHCID 8471—
生成物HCID 178418607HCID 178418607—

反応手順

A mixture containing 3.48 g of 3-(3-tetrahydropyr-2-yloxyprop-1-en-1-yl)-4-hydroxy-6-pivaloylaminopyrrolo[2,3-d]pyrimidine, 3.12g (1.2 equiv.) of diethyl N-(4-iodobenzoyl)glutamate, 546 mg (20%) of tris-(2-methylphenyl)phosphine, 201 mg (10%) of palladium acetate and 85.5 mg (5%) of cuprous iodide in 15 ml of triethylamine and 240 ml of acetonitrile is heated at reflux under nitrogen. After 12 hours., 1.17 g of diethyl N-(4-iodobenzoyl)glutamate are added and the reaction mixture is heated at reflux under nitrogen for an additional 12 hours. The reaction mixture then is concentrated under reduced pressure and the residue chromatographed on silica gel, eluting with 20:1 ethyl acetate:hexane. (Any recovered starting material can be recycled through the foregoing procedure.) The concentrated material is dissolved in 1:5 ethyl acetate:ether and this solution is refrigerated for 15 hours. The solid which forms is collected by filtration, washed with cold ethyl acetate and dried to yield diethyl N-[ 4-(1-(tetrahydropyr-2-yloxy)-3-(4-hydroxy-6 -pivaloylaminopyrrolo[2,3-d]pyrimidin-3-yl)prop-2-en-2yl)benzoyl]glutamate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05344932
出典データセットuspto-grants-1994_09
ORD IDord-a02c36489604445b8f03746b8a5a3991
出典メモuspto-grants-1994_09