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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 408692생성일: 2026년 10월 25일

Formic Acid → 6-chloro-5-pyrrolidin-1-yl-1H-benzoimidazole

https://huagongshe.com/reaction/408692

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참여 물질

역할이름HCID투입량
반응물Formic AcidHCID 284—
반응물4-Chloro-2-nitro-5-(1-pyrrolidinyl)anilineHCID 3613709—
반응물Tin dichloride dihydrateHCID 43835034—
생성물6-chloro-5-pyrrolidin-1-yl-1H-benzoimidazoleHCID 6693743470%

반응 조건

온도130 °C

반응 단계

Formic acid (2.9 mL) was added to a mixture of 4-chloro-2-nitro-5-pyrrolidin-1-yl-phenylamine (0.240 g, 1.00 mmol) and SnCl2.H2O (0.680 g, 3.00 mmol), and the mixture was heated to 130° C. in a microwave reactor for 5 min. Six reactions were performed on the same scale. The combined crude mixture was filtered and washed with EtOAc (100 mL). The organic layer was treated with water (25 mL) and neutralized with aqueous 6M NaOH. The aqueous layer was extracted with EtOAc (3×30 mL). The combined organic layers were washed with brine (50 mL), dried, filtered, and concentrated under reduced pressure. The residue was triturated with EtOAc and the solid was collected to yield the titled compound (1.08 g, 70%) as the formate salt. MS (ESI/CI): mass calcd. for C11H12ClN3, 221.1; m/z found, 222.1 [M+H]+. 1H NMR (400 MHz, DMSO-d6): 12.84-12.16 (br s, 1H), 8.13 (s, 1H), 8.11 (s, 1H), 7.59 (s, 1H), 7.20 (s, 1H), 3.20 (t, J=6.3 Hz, 4H), 2.06-1.66 (m, 4H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08759345B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-6527be80a611453c8b9449ac1690f571
출처 메모uspto-grants-2014_06