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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 369863생성일: 2026년 10월 25일

3-Chloroaniline → 4-(3-chloroanilino)-6-ethoxycarbonyl-7H-pyrrolo[2,3-d]pyrimidine

https://huagongshe.com/reaction/369863

반응식

참여 물질

역할이름HCID투입량
반응물3-ChloroanilineHCID 7932—
반응물Ethyl 4-chloro-7H-pyrrolo[2,3-d]pyrimidine-6-carboxylateHCID 21262606—
반응물Isopropanol hexaneHCID 21585144—
용매1-ButanolHCID 263—
생성물4-(3-chloroanilino)-6-ethoxycarbonyl-7H-pyrrolo[2,3-d]pyrimidineHCID 21262622—

반응 단계

Under an argon atmosphere, 29.0 g (128 mmol) of 4-chloro-6-ethoxycarbonyl-7H-pyrrolo[2,3-d]pyrimidine and 18.0 ml (171 mmol) of 3-chloro-aniline in 430 ml of n-butanol are stirred at 100° C. for 3 hours (almost dissolved after ≈1 hour, then a thick suspension forms). The reaction mixture is cooled to ~50° C., then 400 ml of isopropanol/hexane (1:1) are added thereto. The reaction mixture is then cooled to RT and the product is filtered off and washed with isopropanol and hexane. Stirring from diethyl ether yields the title compound: 1H-NMR (DMSO-d6) 13.0 and 10.53 (2 sb, 2HN), 8.48 (s, 1H), 8.13 (m, 1H), 7.78 (dm, J=8, 1H), 7.76 (s, 1H), 7.45 (t, J=8, 1H), 7.21 (dm, J=8, 1H), 4.37 (q, J=7, 2H), 1.37 (t, J=7, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06140332
출처 데이터셋uspto-grants-2000_10
ORD IDord-e6cf8974b0ed425bb3de8a192aa716e7
출처 메모uspto-grants-2000_10