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HRID 2182818作成日:2026年10月27日

Water → (4-chloro-phenyl)-{4-[hydroxy-(1-trityl-1H-imidazol-4-yl)-methyl]-1-methyl-1H-pyrrol-2-yl}methanone

https://huagongshe.com/reaction/2182818

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物4-Iodo-1-tritylimidazoleHCID 618252—
反応物5-(4-Chlorobenzoyl)-1-methyl-1H-pyrrole-3-carboxaldehydeHCID 22481052—
反応物HCID 178418443HCID 178418443—
溶媒Diethyl EtherHCID 3283—
溶媒DichloromethaneHCID 6344—
生成物(4-chloro-phenyl)-{4-[hydroxy-(1-trityl-1H-imidazol-4-yl)-methyl]-1-methyl-1H-pyrrol-2-yl}methanoneHCID 22481044138.9%

反応手順

To 4.4 g (0.01 mole) 4-iodo-1-tritylimidazole in 80 mL of CH2Cl2 was added dropwise 3.3 mL of 3.0 M ethylmagnesium bromide in Et2O. After stirring for 1 h, a solution of 1.0 g (0.004 mole) of 5-(4-chlorobenzoyl)-1-methyl-1H-pyrrole-3-carboxaldehyde in 10 mL of CH2Cl2 was added dropwise. The resulting reaction mixture was stirred for 2.5 h after which it was poured into water. The solid was filtered off through celite. The organics from the filtrate were separated off, washed with water, brine and dried (Na2SO4). The solvent was evaporated in vacuo to give 3.1 g of (4-chlorophenyl)-{4-[hydroxy-(1-trityl-1H-imidazol-4-yl)-methyl]-1-methyl-1H-pyrrol-2yl}-methanone: CI-MS m/z=559 (M++H). 1HNMR (CDCl3) δ 7.7 (m, 5H) 7.4-7.0 (m, 16H); 6.5 (m, 1H); 3.75 (s, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06897319B2
出典データセットuspto-grants-2005_05
ORD IDord-2d04f7b6ce2b4a2baea1c6d9975d5c5f
出典メモuspto-grants-2005_05