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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 222052생성일: 2026년 10월 25일

1-(3-fluorobenzyl)-5-nitro-1H-indazole → 1-(3-Fluorobenzyl)-1H-indazol-5-amine

https://huagongshe.com/reaction/222052

반응식

참여 물질

역할이름HCID투입량
반응물1-(3-fluorobenzyl)-5-nitro-1H-indazoleHCID 21966490—
촉매IronHCID 23925—
용매Acetic AcidHCID 176—
용매Ethyl AcetateHCID 8857—
생성물1-(3-Fluorobenzyl)-1H-indazol-5-amineHCID 714707376%

반응 단계

5-nitro-1-N-(3-fluorobenzyl)indazole (7.9 g, 29.1 mmol, 1 equiv) and iron (8.13 g, 145.6 mmol, 5 equiv) were mixed in 200 mL acetic acid and 50 mL EtOAc, and were stirred at rt for 36 h. The reaction mixture was filtered through a pad of Celite®. The filtrate was concentrated in vacuo to 10 mL volume. The contents were diluted with water (10 mL) and neutralized with saturated Na2CO3 solution. The solution was extracted with EtOAc (3×500 mL), the combined organic layers dried over MgSO4, filtered, and concentrated in vacuo. The resulting crude material was purified by column chromatography eluting with hexanes/EtOAC (4:1 to 3:1) to give 5-amino-1-N-(3-fluorobenzyl)indazole (5.32 g, 76%) as a light brown solid. 1H-NMR (DMSO-d6) δ 7.72 (s, 1H), 7.22-7.36 (m, 2H), 6.87-7.05 (m, 3H), 6.70-6.77 (m, 2H), 5.48 (s, 2H), 4.78 (br s, 2H); LCMS RT=1.66 min; [M+H]+=242.2.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08207172B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-be7a5ae511a74c2ba7958be2a030c5b4
출처 메모uspto-grants-2012_06