참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Piperazine, 1-(1-adamantyl)- | HCID 35373 | — |
| 반응물 | 2,4-Diamino-6-chloropyrimidine | HCID 67432 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | 1-(1-Adamantyl)-4-(2,6-diamino-4-pyrimidinyl)-piperazine | HCID 18946300 | 80.2% |
반응 단계
A mixture of 2,6-diamino-4-chloropyrimidine (0.43 g, 3.0 mmol) and 1-(1-adamantyl)-piperazine (0.66 g, 3.0 mmol) in ethanol (30 ml) was heated in a sealed tube at 170° C. for 3 hours. After cooling the solvent was removed, the solid residue was dissolved in water (45 ml) and acidified to pH=3 with conc. HCl. The obtained mixture was heated to 50° C. the insolubles were filtered off and the clear solution was rendered alkaline with 10N NaOH under stirring and cooling. The precipitated crystals were collected, washed with water until neutral and dried. In this manner 0.79 g of the title compound was obtained in the form of its monohydrate, yield: 76.6%, mp. 265°-268° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05380724 |
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| 출처 데이터셋 | uspto-grants-1995_01 |
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| ORD ID | ord-ffaac1866e2e41fd8560fdae32cb8b29 |
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| 출처 메모 | uspto-grants-1995_01 |
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