Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 83605생성일: 2026년 10월 23일
N-Methylbenzylamine → N-benzyl-1-(1-(4-chlorobenzyl)-1H-indole-2-carbonyl)-N-methylpiperidine-4-carboxamide
https://huagongshe.com/ko/reaction/83605
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | N-Methylbenzylamine | HCID 7669 | — |
| 반응물 | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| 반응물 | 1-Hydroxybenzotriazole | HCID 75771 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | 1-(1-(4-chlorobenzyl)-1H-indole-2-carbonyl)piperidine-4-carboxylic acid | HCID 57385796 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | N-benzyl-1-(1-(4-chlorobenzyl)-1H-indole-2-carbonyl)-N-methylpiperidine-4-carboxamide | HCID 66571095 | — |
반응 단계
1-(1-(4-chlorobenzyl)-1H-indole-2-carbonyl)piperidine-4-carboxylic acid (150 mg, 0.378 mmol), 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide (145 mg, 0.756 mmol), and 1-Hydroxybenzotriazole (102 mg, 0.756 mmol) were dissolved in 2.0 mL of DCM. The reaction was allowed to stir for 10 minutes before N,N-Diisopropylethylamine (132 μL, 0.756 mmol) and N-methyl-1-phenylmethanamine (45.8 mg, 0.378 mmol) were added as a 1.0 mL DCM solution. The reaction was allowed to stir overnight. The reaction was diluted with water and ethyl acetate. The layers were separated and the organic layer was washed with another aliquot of water. The ethyl acetate layer was washed with 1N HCl followed by saturated sodium bicarbonate then saturated sodium chloride. The organic layer was dried over magnesium sulfate, filtered and concentrated. The crude material was triturated with methanol and filtered under vacuum to obtain pure product as a white solid. Yield: 63.7 mg (White solid)
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US08846684B2 |
|---|
| 출처 데이터셋 | uspto-grants-2014_09 |
|---|
| ORD ID | ord-c8c8a21661a646478d543c99802c78ca |
|---|
| 출처 메모 | uspto-grants-2014_09 |
|---|