Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Formic Acid → 7-Chloro-1H-benzo[d]imidazol-5-amine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Formic Acid | HCID 284 | — |
| 반응물 | Formamide | HCID 713 | — |
| 반응물 | 6-Chloro-2,4-dinitroaniline | HCID 19052 | — |
| 반응물 | HCID 178522168 | HCID 178522168 | — |
| 촉매 | Palladium | HCID 23938 | — |
| 용매 | Hydrochloric Acid | HCID 313 | — |
| 용매 | Ethanol | HCID 702 | — |
| 용매 | Acetic Anhydride | HCID 7918 | — |
| 생성물 | 7-Chloro-1H-benzo[d]imidazol-5-amine | HCID 178507673 | — |
반응 단계
Methanolic solution of 6-chloro-2,4-dinitroaniline (2.4 g, 11 mmol) was stirred overnight with 100 mg of 10% Pd/C under H2. Reaction mixture was filtered and concentrated in vacuo to provide an oil which was dissolved in 10 ml of acetic anhydride and 10 ml of formic acid and stirred at reflux for 12 h. The reaction mixture was concentrated in vacuo, yielding a brown oil which was characterized as 4-chloro-6-foramidylbenzimidazole in NMR analysis. The formamide was dissolved in 20 ml of HCl sat'd EtOH and stirred for 3h at 25° C. The reaction mixture was purified in column chromatography (5% MeOH/EtOAc) to provide 0.89 g (5.3 mmol, 48% overall) of the desired product.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06316637B1 |
| 출처 데이터셋 | uspto-grants-2001_11 |
| ORD ID | ord-98b5b6c4ca6e4c908c7280faa5b61774 |
| 출처 메모 | uspto-grants-2001_11 |