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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1014425생성일: 2026년 10월 26일

2-Amino-5-bromobenzamide → 5-bromo-2-({2-chloro-7-[(4-methylphenyl)sulfonyl]-7H-pyrrolo[2,3-d]pyrimidin-4-yl}amino)benzamide

https://huagongshe.com/reaction/1014425

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참여 물질

역할이름HCID투입량
반응물2-Amino-5-bromobenzamideHCID 5019271—
반응물2,4-dichloro-7-tosyl-7H-pyrrolo[2,3-d]pyrimidineHCID 53486828—
생성물5-bromo-2-({2-chloro-7-[(4-methylphenyl)sulfonyl]-7H-pyrrolo[2,3-d]pyrimidin-4-yl}amino)benzamideHCID 86644194—

반응 단계

Using General Protocol II and starting with 2,4-dichloro-7-[(4-methylphenyl)sulfonyl]-7H-pyrrolo[2,3-d]pyrimidine (4.0 g, 11.7 mmol) and 2-amino-5-bromobenzamide (7.6 g, 35.2 mmol), 5-bromo-2-({2-chloro-7-[(4-methylphenyl)sulfonyl]-7H-pyrrolo[2,3-d]pyrimidin-4-yl}amino)benzamide was isolated as a yellow solid (2.1 g, 35% Yield); 1H NMR (400 MHz, DMSO-d6) δppm 2.36 (s, 3 H), 6.70 (d, J=3.66 Hz, 1 H), 7.46 (d, J=8.42 Hz, 2 H), 7.74-7.78 (m, 2 H), 7.88 (s, 1 H), 7.97 (d, J=8.42 Hz, 2 H), 8.00 (d, J=2.20 Hz, 1 H), 8.35 (d, J=8.79 Hz, 1 H), 8.39 (s, 1 H), 12.16 (s, 1 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07981903B2
출처 데이터셋uspto-grants-2011_07
ORD IDord-bbcf680af59a44d49a2cf4e93383d2e6
출처 메모uspto-grants-2011_07