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HRID 2085085作成日:2026年10月25日

Water → p-t-butyl-N-[6-chloro-5-(o-methoxyphenoxy)-4-pyrimidinyl]benzenesulfonamide

https://huagongshe.com/reaction/2085085

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物HCID 15819130HCID 15819130—
反応物HCID 131721323HCID 131721323—
溶媒Dimethyl SulfoxideHCID 679—
生成物p-t-butyl-N-[6-chloro-5-(o-methoxyphenoxy)-4-pyrimidinyl]benzenesulfonamideHCID 15819129—

反応手順

To a solution of 2 g of 4,6-dichloro-5-(o-methoxyphenoxy)-pyrimidine in 40 ml of DMSO 3.7 g of 4-tert.butylbenzene sulfonamide potassium salt was added. The resulting solution was stirred for 20 h at room temperature. Eventually, the mixture was poured onto 400 ml of water and washed twice with 200 ml of diethyl ether. The organic layers were extracted with 200 ml of water. The combinded aqueous layers were acidified with conc. hydrochloric acid. The mixture was cooled to 0° C. and 100 ml of brine was added. The precipitate that formed was collected and dried to yield 2.7 g of 4-tert.-butyl-N-[6-chloro-5-(o-methoxyphenoxy)-4-pyrimidinyl]-benzene sulfonamide as a white powder. LC-MS: tR=5.80 min, [M+1]+=448.17, [M−1]−=446.21.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06720322B2
出典データセットuspto-grants-2004_04
ORD IDord-b3fc6af0ac56460da8818a4703f94f01
出典メモuspto-grants-2004_04