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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1162575생성일: 2026년 10월 23일

Triphenylphosphine → HCID 178497775, 화합물

https://huagongshe.com/ko/reaction/1162575

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물Diisopropyl diazene-1,2-dicarboxylateHCID 75555—
반응물3-({Cyclopentyl-[4-(4-hydroxy-phenyl)-pyrimidin-2-yl]-amino}-methyl)-benzoic acid methyl esterHCID 136352437—
반응물HCID 178461406HCID 178461406—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물HCID 178497775HCID 17849777532%

반응 단계

To a THF (2 mL) solution of 3-({cyclopentyl-[4-(4-hydroxy-phenyl)-pyrimidin-2-yl]-amino}-methyl)-benzoic acid methyl ester (39 mg, 0.10 mmol) (prepared in Example 172) was added cis-4-methyl-cyclohexanol (11 mg, 0.10 mmol) and triphenylphosphine (25 mg, 0.10 mmol). After the mixture was cooled 5 min. in an ice bath, diisopropyl azodicarboxylate (DIAD, 19.1 μL, 0.10 mmol) was added. The solution was stirred at room temperature until complete. Water was added, and the mixture was extracted with ethyl acetate (3×2 mL). The ethyl acetate layer was dried over Na2SO4 and concentrated. Purification was carried out by silica gel chromatography eluting with hexanes/ethyl acetate 9:1 then 4:1 to give 16 mg of 3-[(cyclopentyl-{4-[4-(trans-4-methyl-cyclohexyloxy)-phenyl]-pyrimidin-2-yl}-amino)-methyl]-benzoic acid methyl ester. LCMS m/z: 501 (M+1)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07820704B2
출처 데이터셋uspto-grants-2010_10
ORD IDord-855adcf56f8643cbb6727d45e23fb1f9
출처 메모uspto-grants-2010_10