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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 829생성일: 2026년 10월 23일

Hydrochloric Acid → Methyl 2-[[[[(4-Methoxy-6-methyl-1,3,6-triazin-2-yl)amino]carbonyl]amino]sulfonyl]-1-methyl-1H-pyrrole-3-carboxylate

https://huagongshe.com/ko/reaction/829

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물Carbamic acid, (4-methoxy-6-methyl-1,3,5-triazin-2-yl)-, phenyl esterHCID 11448329—
반응물Methyl 2-(aminosulfonyl)-1-methyl-1H-pyrrole-3-carboxylateHCID 15790330—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
생성물Methyl 2-[[[[(4-Methoxy-6-methyl-1,3,6-triazin-2-yl)amino]carbonyl]amino]sulfonyl]-1-methyl-1H-pyrrole-3-carboxylateHCID 19693847—

반응 단계

Methyl 2-(aminosulfonyl)-1-methyl-1H-pyrrole-3-carboxylate (0.10 g, 0.46 mmol) and 0.13 g (0.50 mmol) of phenyl (4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamate were combined in 2 mL of acetonitrile and 0.075 mL of DBU was added and the resulting amber solution was stirred at ambient temperature for 30 min. The reaction mixture was diluted with 15 mL of water and acidified with 0.5 mL 1N HCl and the resulting precipitate was collected by filtration and rinsed successively with water and ether, then dried to afford 0.13 g oil the title compound as a white solid, m.p. 189°-190° C. (dec).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05723410
출처 데이터셋uspto-grants-1998_03
ORD IDord-a5a19d2e3ccc4cb7bff13f06f043ffc0
출처 메모uspto-grants-1998_03