Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
2-Chloroadenosine → 2-[6-Amino-2-(indan-2-ylamino)-purin-9-yl]-5-hydroxymethyl-tetrahydro-furan-3,4-diol
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 2-Chloroadenosine | HCID 8974 | — |
| 반응물 | Isoamyl Alcohol | HCID 31260 | — |
| 반응물 | 2-Aminoindane | HCID 76310 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 2-[6-Amino-2-(indan-2-ylamino)-purin-9-yl]-5-hydroxymethyl-tetrahydro-furan-3,4-diol | HCID 15690127 | — |
반응 단계
A mixture of 1.0 g of 2-chloroadenosine, 1.2 g of 2-indanylamine, and 1.6 ml of diisopropylethylamine and 1.0 ml of isoamyl alcohol is refluxed for 16 hours. The reaction mixture is diluted with ethyl acetate and washed with saturated sodium bicarbonate solution. After drying over magnesium sulfate the solvent is removed in vacuo and the residue is chromatographed on silica gel with 10:1 methylene chloride/ammonia saturated methanol as the eluent. The resulting product is recrystallized from methanol to afford 2-(2-indanylamino)-adenosine melting at 129°-132°.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05034381 |
| 출처 데이터셋 | uspto-grants-1991_07 |
| ORD ID | ord-82de9719748d4c5bb7e8257c39e9438c |
| 출처 메모 | uspto-grants-1991_07 |