Triphenylphosphine → tert-butyl 3-((4-amino-3-((3,5-dimethoxyphenyl)ethynyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)methyl)pyrrolidine-1-carboxylate

HRID 516149노트

반응식

HRID 516149 반응식
CC(OC(/N=N/C(OC(C)C)=O)=O)C.[CH3:15][O:16][C:17]1[CH:18]=[C:19]([C:25]#[C:26][C:27]2[C:35]3[C:30](=[N:31][CH:32]=[N:33][C:34]=3[NH2:36])[NH:29][N:28]=2)[CH:20]=[C:21]([O:23][CH3:24])[CH:22]=1.[C:37]([N:44]1[CH2:48][CH2:47][CH:46]([CH2:49]O)[CH2:45]1)([O:39][C:40]([CH3:43])([CH3:42])[CH3:41])=[O:38].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>C1COCC1>[NH2:36][C:34]1[N:33]=[CH:32][N:31]=[C:30]2[N:29]([CH2:49][CH:46]3[CH2:47][CH2:48][N:44]([C:37]([O:39][C:40]([CH3:41])([CH3:43])[CH3:42])=[O:38])[CH2:45]3)[N:28]=[C:27]([C:26]#[C:25][C:19]3[CH:18]=[C:17]([O:16][CH3:15])[CH:22]=[C:21]([O:23][CH3:24])[CH:20]=3)[C:35]=12

참가 물질

6

실험 절차

DIAD (197 μl) was added to a suspension of 3-((3,5-dimethoxyphenyl)ethynyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (148 mg) obtained in Example 1 (Step 1), N-Boc-3-hydroxymethylpyrrolidine (154 mg), polymer supported triphenylphosphine (up to 3.0 mmol/g, 334 mg) in THF (5.0 ml), followed by stirring at room temperature for 3 hours. The insoluble matter was filtered out, and the solvent was distilled off under reduced pressure. The resulting residue was purified by basic silica gel column chromatography (developing solvent: hexane/ethyl acetate) to obtain the title compound as a colorless, amorphous substance (94.5 mg). Physical properties: m/z [M+H]+ 479.1

후처리

  1. filtrationThe insoluble matter was filtered out
  2. distillationthe solvent was distilled off under reduced pressure
  3. customThe resulting residue was purified by basic silica gel column chromatography (developing solvent: hexane/ethyl acetate)

출처 및 근거

ORD 기록
ord-2a7e46a768fa4cbd8bd7d7a99f47d6ff
출처 데이터셋
uspto-grants-2015_08
특허 번호
US09108973B2

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