참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Phosgene | HCID 6371 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Pyrrolidine | HCID 31268 | — |
| 반응물 | 6-(furan-2-yl)-9H-purin-2-amine | HCID 178508247 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 6-(2-Furyl)-9-(1-pyrrolidinylcarbonyl)-9H-purine-2-amine | HCID 59834977 | 62% |
반응 단계
A solution of pyrrolidine (50 mL, 0.6 mmol) in toluene (2 mL) was treated with a solution of phosgene in toluene (0.31 mL, 1.93-M, 0.6 mmol), heated at 80° C. for 30 mins, cooled and concentrated in vacuo. The residue was dissolved in THF (2 mL) and added to a solution of 6-(2-furyl)-1H-purine-2-amine (100 mg, 0.5 mmol) and Et3N (83 mL, 0.6 mmol) in DMP (0.5 mL), stirred at 60° C. for 16 h, poured into water and extracted with EtOAc. The combined organic phase was dried (MgSO4), concentrated in vacuo and the resulting solid triturated with EtOAc/heptane and filtered to give the title compound (92 mg, 62%) as a cream solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07452894B2 |
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| 출처 데이터셋 | uspto-grants-2008_11 |
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| ORD ID | ord-aa7f95a0fb27463884a087d55b99382d |
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| 출처 메모 | uspto-grants-2008_11 |
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