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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1263538생성일: 2026년 10월 27일

Acetic Acid → 2-[(4-methyl-1H-benzimidazol-2-yl)methyl]-1H-benzimidazol-4-ylamine dihydrochloride

https://huagongshe.com/reaction/1263538

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물2,3-DiaminotolueneHCID 17593—
반응물Diethyl malonimidateHCID 73106—
반응물3-Nitro-1,2-phenylenediamineHCID 4359525—
용매Hydrochloric AcidHCID 313—
생성물2-[(4-methyl-1H-benzimidazol-2-yl)methyl]-1H-benzimidazol-4-ylamine dihydrochlorideHCID 1861687966.6%

반응 단계

The following components were reacted according to General Procedure 1, above: 3-nitro-1,2-phenylenediamine (0.5 g; 3.26 mmoles), 3-methyl-1,2-phenylenediamine (0.4 g; 3.26 mmoles), diethyl malonimidate dihydrochloride (1.1 eq.; 0.83 g; 3.60 mmoles) and acetic acid (25 mL). The crude mixture of three compounds was then reduced according to General Procedure 2, above. The crude solid product was taken up in 10 mL of dilute HCl, purified by preparative HPLC (15 to 75% acetonitrile (with 0.1% TFA) over 60 minutes) and converted to the HCl salt by three freeze drying cycles with dilute HCl. This procedure gave 0.42 g of pure 2-[(4-methyl-1H-benzimidazol-2-yl)methyl]-1H-benzimidazol-4-ylamine dihydrochloride in 37% yield. It had MS: m/z=278.2 [N+1] amu and gave one peak on HPLC at both 210 and 280 nm (12.01 minutes using the JWTFACN gradient).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06541486B1
출처 데이터셋uspto-grants-2003_04
ORD IDord-3409410321724b4ba1a2df2c75a03243
출처 메모uspto-grants-2003_04