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HRID 644952作成日:2026年10月26日

Imidazole → HCID 23525647、化合物

https://huagongshe.com/reaction/644952

反応式

関与物質

役割名称HCID仕込み量
反応物ImidazoleHCID 795—
反応物TriphenylphosphineHCID 11776—
反応物ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
反応物Tert-Butyl 4-{4-Chloro-2-[(1R)-1-Hydroxyethyl]Phenyl}-3,6-Dihydropyridine-1(2H)-CarboxylateHCID 68519018—
触媒Zinc azideHCID 178514646—
溶媒DichloromethaneHCID 6344—
生成物HCID 23525647HCID 23525647—

反応手順

A solution of diethyl azodicarboxylate (49.6 mL, 0.315 mol) was added dropwise to a stirred mixture of tert-butyl 4-{4-chloro-2-[(1R)-1-hydroxyethyl]phenyl}-3,6-dihydropyridine-1(2H)-carboxylate (26.7 g, 78.9 mmol), Zn(N3)2.2Py (prepared according to: Viaud, M-C; Rollin, P. Synthesis 1990:130-131) (48.5 g, 0.158 mol), triphenylphosphine (82.7 g, 0.315 mol) and imidazole (21.5 g, 0.315 mol) in dichloromethane at approximately 0° C. After the addition, the resulting mixture was allowed to warm to ambient temperature and stirred vigorously for 3 days. The reaction mixture was filtered through a short column of silica gel eluted with the appropriate volume of dichloromethane to remove excess salts and polar byproducts. The filtrate was concentrated in vacuo and the crude residue was purified by flash chromatography on silica gel (12.5% ethyl acetate/hexanes as eluent) to furnish the title compound as a viscous pale yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07700778B2
出典データセットuspto-grants-2010_04
ORD IDord-9817cd2b1e83400ea35ce1dd8e1b184e
出典メモuspto-grants-2010_04