Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Triethylamine → N-[2-(Phenylsulfonyl)ethyl]-1-piperidineethanamine maleate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | ((2-Chloroethyl)sulphonyl)benzene | HCID 13646 | — |
| 반응물 | N-(2-Aminoethyl)piperidine | HCID 33944 | — |
| 반응물 | Maleic Acid | HCID 444266 | — |
| 용매 | Methanol | HCID 887 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | N-[2-(Phenylsulfonyl)ethyl]-1-piperidineethanamine maleate | HCID 70360543 | 60.78% |
반응 단계
A mixture of 40.94 g (0.20 mole) of [(2-chloroethyl)sulfonyl]benzene, 27.85 g (0.217 mole) of N-(2-aminoethyl)piperidine and 28.0 g (0.277 mole) of triethylamine in 800 ml of acetonitrile was stirred at room temperature overnight. The solvent was removed in vacuo, and the residue was partitioned between methylene chloride and dilute sodium hydroxide. The methylene chloride solution was dried over magnesium sulfate, and the solvent was removed in vacuo. The residue was dissolved in methanol, a solution of 2 equivalents of maleic acid in methanol was added, and the product crystallized from the solution at room temperatue to give 64.35 g (60.78%) of title compound as a white crystalline solid, mp 154°-155.5° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04895840 |
| 출처 데이터셋 | uspto-grants-1990_01 |
| ORD ID | ord-02a04086823f4a4e8450854c0a958793 |
| 출처 메모 | uspto-grants-1990_01 |