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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 75669생성일: 2026년 10월 23일

2,6-Lutidine → N-{3-[1-(2-fluoro-4-iodophenyl)-3,6,8-trimethyl-2,4,7-trioxo-1,2,3,4,7,8-hexahydro-pyrido[2,3-d]pyrimidin-5-ylamino]phenyl}methanesulfonamide

https://huagongshe.com/ko/reaction/75669

반응식

참여 물질

역할이름HCID투입량
반응물2,6-LutidineHCID 7937—
반응물DimethylacetamideHCID 31374—
반응물N-(3-Aminophenyl)methanesulfamideHCID 2734262—
반응물Trifluoromethanesulfonic acid 1-(2-fluoro-4-iodophenyl)-3,6,8-trimethyl-2,4,7-trioxo-1,2,3,4,7,8-hexahydro-pyrido[2,3-d]pyrimidin-5-yl esterHCID 59717446—
용매Methanol--water (1/1)HCID 22242641—
생성물N-{3-[1-(2-fluoro-4-iodophenyl)-3,6,8-trimethyl-2,4,7-trioxo-1,2,3,4,7,8-hexahydro-pyrido[2,3-d]pyrimidin-5-ylamino]phenyl}methanesulfonamideHCID 5971722098.3%

반응 조건

온도130 °C

반응 단계

To trifluoromethanesulfonic acid 1-(2-fluoro-4-iodophenyl)-3,6,8-trimethyl-2,4,7-trioxo-1,2,3,4,7,8-hexahydro-pyrido[2,3-d]pyrimidin-5-yl ester 70 (3.00 g) obtained in Step 6 and N-(3-aminophenyl)methanesulfonamide 44 (1.14 g) were added N,N-dimethylacetamide (6.00 ml) and 2,6-lutidine (0.712 ml), and the mixture was stirred at 130° C. for 4 hrs. After allowing to cool to room temperature, methanol/water [1:2 (volume ratio), 18.0 ml] was added under stirring. The crystals were collected by filtration and dried to give N-{3-[1-(2-fluoro-4-iodophenyl)-3,6,8-trimethyl-2,4,7-trioxo-1,2,3,4,7,8-hexahydro-pyrido[2,3-d]pyrimidin-5-ylamino]phenyl}methanesulfonamide 71 (3.13 g, yield 98%) as a pale-gray solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08835443B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-da8b3023cc66426ca1651be16752627e
출처 메모uspto-grants-2014_09