돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4137생성일: 2026년 10월 23일

Phosgene → 2-(Chloromethyl)-N-[(4,6-dimethoxypyrimidin-2-yl)-aminocarbonyl]benzenesulfonamide

https://huagongshe.com/ko/reaction/4137

반응식

참여 물질

역할이름HCID투입량
반응물PhosgeneHCID 6371—
반응물Sulphonyl diisocyanateHCID 77898—
반응물2-Amino-4,6-dimethoxypyrimidineHCID 118946—
반응물2-(Chloromethyl)-N-(butylaminocarbonyl)benzenesulfonamideHCID 13631887—
반응물2-(Chloromethyl)benzenesulfonyl isocyanateHCID 20152699—
촉매Diazabicyclo(2.2.2)octaneHCID 136165—
용매AcetonitrileHCID 6342—
용매O-XyleneHCID 7237—
생성물2-(Chloromethyl)-N-[(4,6-dimethoxypyrimidin-2-yl)-aminocarbonyl]benzenesulfonamideHCID 1336461769.6%

반응 단계

A solution of 2-(chloromethyl)-N-(butylaminocarbonyl)benzene sulfonamide (1.33 g, 4.38 mmol) and diazabicyclo[2.2.2]octane (5 mg) in xylene (12 ml) was heated at reflux and contacted in portions with phosgene (1.0 ml. condensed phase). After 2.0 hrs at reflux, the mixture was cooled to room temperature, decanted, and volatiles were removed to give 1.56 g of crude product. The IR spectrum of 2-(chloromethyl)benzenesulfonyl isocyanate featured a strong band at 2250 cm-1. The crude sulfonyl isocyanate was contacted with acetonitrile (10 ml) and 2-amino-4,6-dimethoxypyrimidine (0.68 g, 4.4 mmol) and stirred for 16 hrs. Filtration gave 1.18 g of white solid, mp 192°-193°. The sample was dissolved in 0.5N NaOH, filtered and pH adjusted to 6.5. The mixture was cooled and filtered and the solid washed with ice water and dried to give 0.90 g of white solid. 1H nmr δDMSO-d6TMS 12.7 (brd s, 10.50 (s, 1H) 8.13-7.97 (m, 1H), 7.73-7.40 (m, 3H), 5.90 (s, 1H), 5.10 (s, 2H), 3.87 (s, 6H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04723990
출처 데이터셋uspto-grants-1988_02
ORD IDord-7101f12d796b4a7697ca6546a96de61b
출처 메모uspto-grants-1988_02