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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1097718생성일: 2026년 10월 27일

Triphenylphosphine → 3-Butyl-8-chloro-1-[4-(3-phenyl-5-isoxazolyl)butyl]-3,7-dihydro-1H-purine-2,6-dione

https://huagongshe.com/reaction/1097718

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참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물1,2-Bis(phenylmethyl) 1,2-diazenedicarboxylateHCID 75557—
반응물3-butyl-8-chloro-7-(2-propen-1-yl)-3,7-dihydro-1H-purine-2,6-dioneHCID 59299582—
반응물4-(3-Phenyl-5-isoxazolyl)-1-butanolHCID 59395604—
용매TetrahydrofuranHCID 8028—
생성물3-Butyl-8-chloro-1-[4-(3-phenyl-5-isoxazolyl)butyl]-3,7-dihydro-1H-purine-2,6-dioneHCID 5939546335.8%

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온도0 °C

반응 단계

3-Butyl-8-chloro-7-(2-propen-1-yl)-3,7-dihydro-1H-purine-2,6-dione (100 mg, 0.354 mmol) and 4-(3-phenyl-5-isoxazolyl)-1-butanol (77 mg, 0.355 mmol) were dissolved in dry THF (4 ml) under nitrogen. A solution of dibenzyl azodicarboxylate (94%, 224 mg, 0.708 mmol) in dry THF (2 ml) was added. The mixture was cooled to 0° C. and a solution of triphenylphosphine (185 mg, 0.708 mmol) in dry THF (1 ml) was added. The mixture was stirred for 20 min at 0° C. then at room temperature overnight. The mixture was degassed then stirred with morpholine (0.308 ml) and tetrakis(triphenylphosphine)palladium(0) (82 mg) for 4.5 h. A further 60 mg of tetrakis(triphenylphosphine)palladium(0) was added and stirring continued overnight. The reaction was worked up by partition between EtOAc and 2M HCl, the organic phase evaporated and purified by aminopropyl SPE (5 g) washing with THF-MeOH (1:1), MeOH and eluting with DCM-MeOH (1:1) containing 5% AcOH. Further purification by MDAP afforded the title compound (56 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08143264B2
출처 데이터셋uspto-grants-2012_03
ORD IDord-1b6ecf0713db43e3a1daa254858a9817
출처 메모uspto-grants-2012_03