Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1270919생성일: 2026년 10월 26일
3-(4-Amino-3-methoxyphenyl)-7-iodofuro[3,2-c]pyridin-4-amine → N-[4-(4-amino-7-iodofuro[3,2-c]pyridin-3-yl)-2-methoxyphenyl]-1-methyl-1H-benzimidazole-2-carboxamide
https://huagongshe.com/reaction/1270919
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 3-(4-Amino-3-methoxyphenyl)-7-iodofuro[3,2-c]pyridin-4-amine | HCID 18450709 | — |
| 반응물 | 1-Methyl-1H-benzimidazole-2-carbonyl chloride | HCID 20543227 | — |
| 용매 | Pyridine | HCID 1049 | — |
| 생성물 | N-[4-(4-amino-7-iodofuro[3,2-c]pyridin-3-yl)-2-methoxyphenyl]-1-methyl-1H-benzimidazole-2-carboxamide | HCID 18451295 | 105.8% |
반응 단계
A solution of 3-(4-amino-3-methoxyphenyl)-7-iodofuro[3,2-c]pyridin-4-amine (1.50 g, 3.94 mmol) in pyridine (18 mL) was cooled to 0° C. and 1-methyl-1H-benzo[d]imidazole-2-carbonyl chloride (0.874 g, 3.33 mmol) was added. The mixture was stirred for 15 minutes at 0° C. and then allowed to rise to ambient temperature over an eighteen hour time period. The solvent was removed in vacuo and the residue was suspended in water (50 mL) and brought to pH 12 with 0.1 N aqueous sodium hydroxide. The suspension was extracted with dichloromethane (4×25 mL) and the combined organic layers were washed with brine (25 mL) and dried over anhydrous magnesium sulfate. The solvent was removed in vacuo to give the title compound (1.90 g, 90%) as a yellow solid. 1H NMR (DMSO-d6, 400 MHz.)δ 10.18 (s, 1H), 8.49 (d, 1H), 8.14 (s, 1H), 8.08 (s, 1H), 7.85 (d, 1H), 7.76 (d, 1H), 7.46 (t, 1H), 7.39 (t, 1H), 7.30 (s, 1H), 7.19 (d, 1H), 5.77–5.89 (b, 2H), 4.24 (s, 3H), 4.03 (s, 3H); RP-HPLC (Conditions d) Rt 11.89 min.; MS: MH+ 540.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07202363B2 |
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| 출처 데이터셋 | uspto-grants-2007_04 |
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| ORD ID | ord-a03d437eddd4489399c09bc23c4ab2e4 |
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| 출처 메모 | uspto-grants-2007_04 |
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