Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Acetone → Methyl 2-[2-Hydroxy-3-[N-[2-[N-(4-methylphenylsulfonyl)amino]ethyl]amino]propoxy]benzoate Oxalate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Acetone | HCID 180 | — |
| 반응물 | Oxalic Acid | HCID 971 | — |
| 반응물 | Methyl 2-(oxiran-2-ylmethoxy)benzoate | HCID 279510 | — |
| 반응물 | N-(2-Aminoethyl)-4-methylbenzenesulfonamide | HCID 301318 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | Methyl 2-[2-Hydroxy-3-[N-[2-[N-(4-methylphenylsulfonyl)amino]ethyl]amino]propoxy]benzoate Oxalate | HCID 13732868 | — |
반응 단계
A solution of 2.15 g of N-(2-aminoethyl)-p-toluenesulfonamide (0.1 mole) and 2.08 g of methyl 2-(2,3-epoxypropoxy)benzoate (0.01 mole) in 100 ml of methanol was stored at 25° C. for 4 hours. The methanol was then removed under reduced pressure, leaving an oil (NMR indicated only mono-alkylated product). The oil was then dissolved in 50 ml of methanol and an equimolar quantity of oxalic acid was added to the solution. 50 Ml of acetone was added, and the product crystallized upon refrigeration. The product was recrystallization from acetone/methanol (1:1) to yield 1.4 g of product which had a melting point of 165°-166° C. The elemental analysis (CHN) and NMR spectrum were consistent with the assigned structure.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04623652 |
| 출처 데이터셋 | uspto-grants-1986_11 |
| ORD ID | ord-56f42d917c074e938e6e5f2d16399366 |
| 출처 메모 | uspto-grants-1986_11 |