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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 10246생성일: 2026년 10월 24일

Diisopropylethylamine → 4-Methyl-phenyl sulfamic acid-[6-chloro-5-(p-tolyl)-4-pyrimidinyl]-amide

https://huagongshe.com/ko/reaction/10246

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물4,6-Dichloro-5-(4-methylphenyl)pyrimidineHCID 21979554—
반응물4-Methyl-phenyl sulfamic acid amide potassium saltHCID 69512930—
용매Dimethyl SulfoxideHCID 679—
용매MethanolHCID 887—
생성물4-Methyl-phenyl sulfamic acid-[6-chloro-5-(p-tolyl)-4-pyrimidinyl]-amideHCID 2197955262.1%

반응 단계

To 4,6-dichloro-5-p-tolyl-pyrimidine (Referential Example 7) (2.0 g) dissolved in DMSO (35 ml) was added di-isopropyl-ethyl-amine (1.46 ml) followed by addition of 4-methyl-phenyl sulfamic acid amide potassium salt (2.78 g) [prepared from the product described in Referential Example 19 and potassium tert.-butylate in methanol followed by evaporation of the solvent]. The mixture was stirred for 48 h at rt then poured onto water (500 ml) and diethylether (250 ml) was added and the solution was stirred for 30 min. The layers were separated and the water layer was acidified with acetic acid (2.0 ml) and cooled to 0° C. for 1 h. The precipitated product was filtered off and washed with water and diethylether and dried to give 4-methyl-phenyl sulfamic acid-[6-chloro-5-(p-tolyl)-4-pyrimidinyl]-amide (2.02 g). tR=5.00 min (LC); [M+H]+=389.11 (ES+);

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07094781B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-74338b5aed30449facdcc0ace8215f09
출처 메모uspto-grants-2006_08