Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Triethylamine → 4-amino-N-(1-ethyl-piperidin-4-yl)-benzamide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 1-Ethylpiperidin-4-amine | HCID 3734990 | — |
| 반응물 | 4-Amino-benzoic acid benzotriazol-1-yl ester | HCID 53844583 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 4-amino-N-(1-ethyl-piperidin-4-yl)-benzamide | HCID 54915895 | 84% |
반응 단계
To a mixture of 1.0424 g (4.1 mmole) of 4-amino-benzoic acid benzotriazol-1-yl ester and 8 mL of dry tetrahydrofuran at 0 degrees was added 0.5257 g (4.1 mmole) of 4-amino-1-ethylpiperidine followed by 1.0372 g (10.3 mmole) of triethylamine. The cooling bath was removed and the mixture stirred at room temperature for 65 minutes. Volatiles were removed under reduced pressure and the residue taken up in ethyl acetate, and the organic layer washed twice with 50 mL of 0.5 M sodium carbonate, 50 mL water, and then 50 mL brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure to give 0.8522 g 4-amino-N-(1-ethyl-piperidin-4-yl)-benzamide, as a white solid which was used without further purification.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08003785B2 |
| 출처 데이터셋 | uspto-grants-2011_08 |
| ORD ID | ord-6618e55103764c5285ec53a92e237d85 |
| 출처 메모 | uspto-grants-2011_08 |