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HRID 33259作成日:2026年10月24日

Water → 1-[5-(5-Chloro-thiophen-2-yl)-isoxazol-3-ylmethyl]-5-[2-(2-methoxy-ethoxy)-ethoxymethyl]-1H-pyrazole-3-carboxylic acid ethyl ester

https://huagongshe.com/ja/reaction/33259

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物1-Bromo-3,6-dioxaheptaneHCID 123532—
反応物1-[5-(5-Chloro-thiophen-2-yl)-isoxazol-3-ylmethyl]-5-hydroxymethyl-1H-pyrazole-3-carboxylic acid ethyl esterHCID 60207960—
溶媒DimethylformamideHCID 6228—
生成物1-[5-(5-Chloro-thiophen-2-yl)-isoxazol-3-ylmethyl]-5-[2-(2-methoxy-ethoxy)-ethoxymethyl]-1H-pyrazole-3-carboxylic acid ethyl esterHCID 60207963—

反応手順

To a solution of 100 mg 1-[5-(5-Chloro-thiophen-2-yl)-isoxazol-3-ylmethyl]-5-hydroxymethyl-1H-pyrazole-3-carboxylic acid ethyl ester in 2 ml DMF 11 mg NaH (60% in mineral oil) were added at RT and stirred for 10 min. Then 100 mg 1-Bromo-2-(2-methoxy-ethoxy)-ethane were added and the mixture was stirred for 16 h. After addition of 5 ml of water the mixture was filtered through a chem elut® cartridge by elution with ethyl acetate and then concentrated under reduced pressure. The crude residue was directly subjected to the next reaction step. Yield: 130 mg.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07429581B2
出典データセットuspto-grants-2008_09
ORD IDord-aee257896bf0442b8728612e6eb28f53
出典メモuspto-grants-2008_09