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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

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참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물2-BromothiazoleHCID 76430—
반응물N-[1-(2-aminoethyl)-4-piperidinyl]-9-[(4-fluorophenyl)methyl]-9H-purin-8-amineHCID 19785318—
용매DimethylacetamideHCID 31374—
생성물9-[(4-fluorophenyl)methyl]-N-[1-[2-(2-thiazolylamino)ethyl)-4-piperidinyl]-9H-purin-8-amineHCID 1978530126.5%

반응 조건

온도130 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05258380
출처 데이터셋uspto-grants-1993_11
ORD IDord-206999dec95643568771f08e87551483
출처 메모uspto-grants-1993_11