Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 256672생성일: 2026년 10월 26일
Sodium Carbonate → 9-[(4-fluorophenyl)methyl]-N-[1-[2-(2-thiazolylamino)ethyl)-4-piperidinyl]-9H-purin-8-amine
https://huagongshe.com/reaction/256672
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Sodium Carbonate | HCID 10340 | — |
| 반응물 | 2-Bromothiazole | HCID 76430 | — |
| 반응물 | N-[1-(2-aminoethyl)-4-piperidinyl]-9-[(4-fluorophenyl)methyl]-9H-purin-8-amine | HCID 19785318 | — |
| 용매 | Dimethylacetamide | HCID 31374 | — |
| 생성물 | 9-[(4-fluorophenyl)methyl]-N-[1-[2-(2-thiazolylamino)ethyl)-4-piperidinyl]-9H-purin-8-amine | HCID 19785301 | 26.5% |
반응 단계
A mixture of 3.3 parts of 2-bromothiazole, 5.55 parts of N-[1-(2-aminoethyl)-4-piperidinyl]-9-[(4-fluorophenyl)methyl]-9H-purin-8-amine, 2.12 parts of sodium carbonate and 18 parts of N,N-dimethylacetamide was stirred and heated for 20 hours at 130° C. After cooling, the reaction mixture was poured onto water and the product was extracted with 4-methyl-2-pentanone. The extract was dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane, methanol and methanol saturated with ammonia, (90:5:5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from acetonitrile. The product was filtered off and dried in high vacuo at 100° C., yielding 1.8 parts (26.5%) of 9-[(4-fluorophenyl)methyl]-N-[1-[2-(2-thiazolylamino)ethyl)-4-piperidinyl]-9H-purin-8-amine; mp. 165.4° C. (compound 172).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05258380 |
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| 출처 데이터셋 | uspto-grants-1993_11 |
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| ORD ID | ord-206999dec95643568771f08e87551483 |
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| 출처 메모 | uspto-grants-1993_11 |
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