Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Iodoethane → 2,6-dichloro-7-ethyl-7H-purine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Iodoethane | HCID 6340 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 2,6-Dichloropurine | HCID 5324412 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 2,6-dichloro-7-ethyl-7H-purine | HCID 21988296 | — |
| 생성물 | 2,6-dichloro-9-ethyl-9H-purine | HCID 21988325 | — |
반응 단계
1.0 g (5.29 mmol) of 2,6-dichloro-purine is dissolved in DMF (20 ml) and treated with 152 mg (80%, 5.3 mmol) of sodium hydride and the mixture is stirred at RT for 0.5 hours. After addition of 0.42 ml (5.3 mmol) of ethyl iodide, the mixture is stirred at 70° C. for 3 hours, diluted with ethyl acetate (100 ml) and extracted with concentrated brine. The organic phase is dried (sodium sulfate) and concentrated and the residue is chromatographed (silica gel, methylene chloride:methanol=19:1). An oily mixture comprising 2,6-dichloro-7-ethyl-7H-purine and 2,6-dichloro-9-ethyl-9H-purine is obtained.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07091346B1 |
| 출처 데이터셋 | uspto-grants-2006_08 |
| ORD ID | ord-66d3e0ffc92349d497cdf78b8c94e762 |
| 출처 메모 | uspto-grants-2006_08 |