Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
2-Chlorobenzimidazole → N-(1-Benzylpiperidin-4-yl)-1H-benzimidazol-2-amine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 2-Chlorobenzimidazole | HCID 78572 | — |
| 반응물 | 1-Benzyl-4-piperidylamine | HCID 415852 | — |
| 생성물 | N-(1-Benzylpiperidin-4-yl)-1H-benzimidazol-2-amine | HCID 16640950 | — |
반응 단계
Combine 2-chloro-1H-benzimidazole (5.0 g, 33 mmol) and 1-benzyl-4-aminopiperidine (14.2 g, 75 mmol) and heat to about 150° C. After 12 hours, cool and partition between water and chloroform, warming if necessary. Separate the layers and add methanol and toluene to the organic layer. Evaporate the organic layer in vacuo to give a solid. Triturate the solid with ethyl acetate, collect by filtration, and dry to give (1H-benzimidazol-2-yl)(1-benzylpiperidin-4-yl)amine: Rf=0.30 (2% triethylamine/10% methanol/ethyl acetate).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06211199B1 |
| 출처 데이터셋 | uspto-grants-2001_04 |
| ORD ID | ord-560697a9c71444b5a7705a1b92fc2c32 |
| 출처 메모 | uspto-grants-2001_04 |