Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 17185생성일: 2026년 10월 24일
Phenyl isocyanate → N-(4-{4-amino-7-[(anilinocarbonyl)amino]thieno[3,2-c]pyridin-3-yl}-2-methoxyphenyl)-1-methyl-1H-indole-2-carboxamide
https://huagongshe.com/ko/reaction/17185
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Phenyl isocyanate | HCID 7672 | — |
| 반응물 | Formamidine | HCID 68047 | — |
| 반응물 | HCID 178487773 | HCID 178487773 | — |
| 용매 | Pyridine | HCID 1049 | — |
| 생성물 | N-(4-{4-amino-7-[(anilinocarbonyl)amino]thieno[3,2-c]pyridin-3-yl}-2-methoxyphenyl)-1-methyl-1H-indole-2-carboxamide | HCID 18451286 | 32% |
반응 단계
To a solution of N-[4-(7-amino-4-{[(1E)-(dimethylamino)methylene]amino}thieno[3,2-c]pyridin-3-yl)-2-methoxyphenyl]-1-methyl-1H-indole-2-carboxamide (0.020 g, 0.040 mmol) in pyridine (1.1 mL) at 0° C. was added phenyl isocyanate (0.0043 mL, 0.040 mmol). The mixture was allowed to warm to ambient temperature, and was stirred at ambient temperature for 12 h. The reaction mixture was concentrated, and the residue was purified by flash column chromatography on silica gel, which had been deactivated with triethylamine (10% by volume of silica gel used), using methanol/dichloromethane as the mobile phase, to afford an intermediate that was then subjected to General Procedure M for formamidine hydrolysis to yield the title compound (0.007 g, 32%) as an off-white foam: 1H NMR (DMSO-d6, 400 MHz) δ 9.52 (s, 1H), 9.07 (s, 1H), 8.58 (s, 1H), 8.09 (s, 1H), 8.06 (d, 1H), 7.73 (m, 2H), 7.60 (d, 1H), 7.49 (d, 2H), 7.36 (s, 1H), 7.30 (m, 4H), 7.14 (m, 2H), 7.00 (t, 1H), 6.10 (br, 2H), 4.04 (s, 3H), 3.93 (s, 3H); MS: (MH)+ 563.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07737160B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-b1e6dbb1d798442580b848f7c0b8e627 |
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| 출처 메모 | uspto-grants-2010_06 |
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