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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 9921생성일: 2026년 10월 23일

3-Chlorobenzoic Acid → 6-(4-[3-Chloro-benzoyl-amino]-phenyl-amino)-9-ethyl-2-(2-hydroxy-ethyl-amino)-9H-purine

https://huagongshe.com/ko/reaction/9921

반응식

참여 물질

역할이름HCID투입량
반응물3-Chlorobenzoic AcidHCID 447—
반응물DiisopropylamineHCID 7912—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
반응물6-(4-amino-phenyl-amino)-9-ethyl-2-(2-hydroxy-ethyl-amino)-9H-purineHCID 21988284—
용매Ethyl AcetateHCID 8857—
용매DimethylacetamideHCID 31374—
생성물6-(4-[3-Chloro-benzoyl-amino]-phenyl-amino)-9-ethyl-2-(2-hydroxy-ethyl-amino)-9H-purineHCID 21988238—

반응 단계

62 mg (0.2 mmol) of 6-(4-amino-phenyl-amino)-9-ethyl-2-(2-hydroxy-ethyl-amino)-9H-purine (prepared according to Example 108), 0.18 g (0.4 mmol) of (benzotriazol-1-yloxy)-tris-(dimethylamino)-phosphonium hexafluorophosphate (BOP), 54 mg (0.4 mmol) of 1-hydroxybenzotriazole (HOBT) and 68 μl of diisopropylamine are stirred in 6 ml of dimethylacetamide at RT for 5 min and then treated with 63 mg (0.4 mmol) of 3-chlorobenzoic acid. After the reaction mixture has been stirred at RT for 30 min, it is diluted with ethyl acetate and washed with water. The crude product is purified by chromatography over silica gel (mobile phase: methylene chloride:methanol=9:1). 6-(4-[3-Chloro-benzoyl-amino]-phenyl-amino)-9-ethyl-2-(2-hydroxy-ethyl-amino)-9H-purine is obtained; FAB-MS: (M+H)+=452; Rf=0.45 (methylene chloride:methanol=9:1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091346B1
출처 데이터셋uspto-grants-2006_08
ORD IDord-070783df20e7489689e0498417256699
출처 메모uspto-grants-2006_08