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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | 2,3-Diaminotoluene | HCID 17593 | — |
| 반응물 | Diethyl malonimidate | HCID 73106 | — |
| 반응물 | 3-Nitro-1,2-phenylenediamine | HCID 4359525 | — |
| 용매 | Hydrochloric Acid | HCID 313 | — |
| 생성물 | 2-[(4-methyl-1H-benzimidazol-2-yl)methyl]-1H-benzimidazol-4-ylamine dihydrochloride | HCID 18616879 | 66.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US06541486B1 |
|---|
| 출처 데이터셋 | uspto-grants-2003_04 |
|---|
| ORD ID | ord-3409410321724b4ba1a2df2c75a03243 |
|---|
| 출처 메모 | uspto-grants-2003_04 |
|---|