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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

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참여 물질

역할이름HCID투입량
반응물3-(4-Amino-3-methoxyphenyl)-7-iodofuro[3,2-c]pyridin-4-amineHCID 18450709—
반응물1-Methyl-1H-benzimidazole-2-carbonyl chlorideHCID 20543227—
용매PyridineHCID 1049—
생성물N-[4-(4-amino-7-iodofuro[3,2-c]pyridin-3-yl)-2-methoxyphenyl]-1-methyl-1H-benzimidazole-2-carboxamideHCID 18451295105.8%

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온도0 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07202363B2
출처 데이터셋uspto-grants-2007_04
ORD IDord-a03d437eddd4489399c09bc23c4ab2e4
출처 메모uspto-grants-2007_04