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2-Chloro-6,7-dimethoxy-4-quinazolinamine → 8-[1-(4-Amino-6,7-dimethoxy-2-quinazolinyl)-3-piperidinyl]-8-azaspiro[4,5]decan-7,9-dione hydrochloride
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-Chloro-6,7-dimethoxy-4-quinazolinamine | HCID 90235 | — |
| 反応物 | 8-(3-Piperidinyl)-8-azaspiro[4,5]decan-7,9-dione | HCID 20556261 | — |
| 溶媒 | Isoamyl Alcohol | HCID 31260 | — |
| 生成物 | 8-[1-(4-Amino-6,7-dimethoxy-2-quinazolinyl)-3-piperidinyl]-8-azaspiro[4,5]decan-7,9-dione hydrochloride | HCID 20556251 | — |
反応手順
The mixture of 3.75 g of 8-(3-piperidinyl)-8-azaspiro[4,5]decan-7,9-dione, 3.59 g of 4-amino-2-chloro-6,7-dimethoxyquinazoline and 100 ml of isoamyl alcohol is stirred and refluxed under nitrogen for 24 hours. It is cooled to 20°, the solids filtered off, washed with isoamyl alcohol and diethyl ether and recrystallized from the mixture of 160 ml of methanol and 110 ml of water, to yield the 8-[1-(4-amino-6,7-dimethoxy-2-quinazolinyl)-3-piperidinyl]-8-azaspiro[4,5]decan-7,9-dione hydrochloride melting at 311°-312° with decomposition.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04309541 |
| 出典データセット | uspto-grants-1982_01 |
| ORD ID | ord-0dc5756a398d43c4bb2551379080d6cd |
| 出典メモ | uspto-grants-1982_01 |