반응식
[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[C:9]1[N:17]=[CH:16][N:15]=[C:14]2[C:10]=1[N:11]=[C:12]([CH2:18][CH3:19])[NH:13]2.[CH:20]1([CH:23](O)[C:24]#[CH:25])[CH2:22][CH2:21]1.Cl[CH2:28][CH:29]=[N:30][OH:31].C(=NO)C.ClN1C(=O)CCC1=O>C(Cl)Cl.CN(C=O)C.C(N(CC)CC)C>[CH:20]1([CH:23]([N:13]2[C:12]([CH2:18][CH3:19])=[N:11][C:10]3[C:14]2=[N:15][CH:16]=[N:17][C:9]=3[C:3]2[CH:4]=[CH:5][C:6]([Cl:8])=[CH:7][C:2]=2[Cl:1])[C:24]2[O:31][N:30]=[C:29]([CH3:28])[CH:25]=2)[CH2:22][CH2:21]1참가 물질
반응물 5
생성물 1
시약·촉매·용매 3
실험 절차
To a stirring solution of the compound of Example 7241 (90 mg, 0.24 mmol; prepared in a manner similar to that of Example 2 using 6-(2,4-dichlorophenyl)-8-ethyl-9H-purine and 3-cyclopropyl-1-propyn-3-ol) in methylene chloride (2 mL) were added chloroacetaldoxime (25 mg, 0.27 mmol) and triethylamine (0.038 mL, 0.27 mmol). (The chloroacetaldoxime used was previously prepared by reacting equimolar amounts of acetaldoxime and N-chlorosuccinimide in DMF, then extracting the product into diethyl ether and washing with water.) The cycloaddition reaction was monitored by TLC and additional amounts of chloroacetaldoxime and triethylamine were added until all the starting material was consumed. The reaction mixture was purified by adding directly to 4 column packed with silica gel and eluting using a gradient of 100% hexane to 25% ethyl acetate in hexane. 72 mg of a white foam was collected. MS (NH3-CI) 428 (M+H+). HRMS: m/e=428.1037 (M+H+, C21H20Cl2N5O). Purity by reverse phase HPLC>97%.
후처리
- extractionextracting the product into diethyl ether
- washwashing with water
- custom) The cycloaddition reaction
- additionwere added until all the starting material
- customwas consumed
- customThe reaction mixture was purified
- additionby adding directly to 4 column
- washeluting
- custom72 mg of a white foam was collected
출처 및 근거
- ORD 기록
- ord-fdec06412b1b465c9b8f576d496f0246
- 출처 데이터셋
- uspto-grants-2002_03
- 특허 번호
- US06362180B1
연결된 노트
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