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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 550895생성일: 2026년 10월 25일

2-Isocyanato-1-methoxy-4-methylbenzene → 3-{4-[3-(2-methoxy-5-methylphenyl)ureido]phenyl}-1H-pyrrolo[2,3-c]pyridine-2-carboxamide

https://huagongshe.com/reaction/550895

반응식

참여 물질

역할이름HCID투입량
반응물2-Isocyanato-1-methoxy-4-methylbenzeneHCID 4141520—
반응물3-(4-aminophenyl)-1H-pyrrolo[2,3-c]pyridine-2-carboxamideHCID 57445351—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물3-{4-[3-(2-methoxy-5-methylphenyl)ureido]phenyl}-1H-pyrrolo[2,3-c]pyridine-2-carboxamideHCID 57445318—

반응 단계

To a solution of 100 mg of 3-(4-aminophenyl)-1H-pyrrolo[2,3-c]pyridine-2-carboxamide in 5 mL of tetrahydrofuran are added dropwise 54.4 μL of 2-methoxy-5-methylphenyl isocyanate. The reaction mixture is stirred for 16 hours at room temperature under an argon atmosphere and then concentrated under reduced pressure. The residue obtained is stirred for 30 minutes in 2 mL of dichloromethane. The suspended solid is filtered off, washed with water and drained by suction. After drying under vacuum, at 40° C., 40 mg of 3-{4-[3-(2-methoxy-5-methylphenyl)ureido]phenyl}-1H-pyrrolo[2,3-c]pyridine-2-carboxamide are obtained, the characteristics of which are as follows:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07947706B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-db5ad32e741b430fb7975fd772da434d
출처 메모uspto-grants-2011_05