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HRID 486636作成日:2026年10月26日

Sodium Glycolate → p-t-butyl-N-[6-(2-hydroxyethoxy)-5-(o-methoxyphenoxy)-4-pyrimidinyl]benzenesulfonamide

https://huagongshe.com/reaction/486636

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium GlycolateHCID 517347—
反応物SodiumHCID 5360545—
反応物p-t-butyl-N-[6-chloro-5-(o-methoxyphenoxy)-4-pyrimidinyl]benzenesulfonamideHCID 15819129—
溶媒Ethylene GlycolHCID 174—
生成物p-t-butyl-N-[6-(2-hydroxyethoxy)-5-(o-methoxyphenoxy)-4-pyrimidinyl]benzenesulfonamideHCID 10983585—

反応条件

温度95 °C

反応手順

886 mg of p-t-butyl-N-[6-chloro-5-(o-methoxyphenoxy)-4-pyrimidinyl]benzenesulfonamide were added to a sodium glycolate solution from 3.0 g of ethylene glycol and 138 mg of sodium. The reaction mixture was stirred at 95° C. under argon for 4 hours. Thereafter, the ethylene glycol was distilled off and the residue was partitioned between ethyl acetate and 1N hydrochloric acid. The organic phase was dried and the solvent was distilled off. The residue was crystallized from diisopropyl ether. There were obtained 870 mg of p-t-butyl-N-[6-(2-hydroxyethoxy)-5-(o-methoxyphenoxy)-4-pyrimidinyl]benzenesulfonamide. M.p. 143°-148° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05292740
出典データセットuspto-grants-1994_03
ORD IDord-b360a1b4b98848529920094915422e2f
出典メモuspto-grants-1994_03