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Ethyl isocyanate → 5-Methoxy-3,6,7,8-tetrahydro-1,3-dimethylcyclopenta[d]pyrazolo[3,4-b]-pyridine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ethyl isocyanate | HCID 8022 | — |
| 反応物 | 3,4-Dimethylpyridine | HCID 11417 | — |
| 反応物 | 4-(1,2,5,6-tetrahydro-1-methyl-4-pyridinyl)-1,3-dimethyl 5-(1H)-pyrazolamine | HCID 13352196 | — |
| 生成物 | 5-Methoxy-3,6,7,8-tetrahydro-1,3-dimethylcyclopenta[d]pyrazolo[3,4-b]-pyridine | HCID 20234981 | — |
反応手順
A mixture of 4-(1,2,5,6-tetrahydro-1-methyl-4-pyridinyl)-1,3-dimethyl-5-(1H)-pyrazolamine (2.06 g; 0.01 mol), 3,4-lutidine (20 ml), ethyl isocyanate (3.16 ml; 0.04 mol), under anhydrous conditions, are heated to the reflux temperature for about 3 hours. The mixture is then cooled to room temperature, concentrated under reduced pressure, washed with ethyl acetate and then with ethyl ether, thus obtaining the product of the title. M.p. 294°-297° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04612318 |
| 出典データセット | uspto-grants-1986_09 |
| ORD ID | ord-253260bd1fa943b7ae013142de06fdeb |
| 出典メモ | uspto-grants-1986_09 |