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Propargyl alcohol → 4-(Methylthio)-6-methoxy-7-(3-hydroxyprop-1-ynyl)quinazoline

HRID 2233266
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HRID 2233266 반응식
[CH3:1][S:2][C:3]1[C:12]2[C:7](=[CH:8][C:9](OS(C(F)(F)F)(=O)=O)=[C:10]([O:13][CH3:14])[CH:11]=2)[N:6]=[CH:5][N:4]=1.[CH2:23]([OH:26])[C:24]#[CH:25]>CN(C)C=O.C(N(CC)CC)C>[CH3:1][S:2][C:3]1[C:12]2[C:7](=[CH:8][C:9]([C:25]#[C:24][CH2:23][OH:26])=[C:10]([O:13][CH3:14])[CH:11]=2)[N:6]=[CH:5][N:4]=1
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참가 물질

5

반응물 2

HCID 7859Propargyl alcoholHCID 867610994-(Methylthio)-6-methoxy-7-(trifluoromethanesulphonyloxy)quinazoline

생성물 1

HCID 686771564-(Methylthio)-6-methoxy-7-(3-hydroxyprop-1-ynyl)quinazoline수율 17%

시약·촉매·용매 2

HCID 8471Triethylamine촉매HCID 6228Dimethylformamide용매

실험 절차

4-(methylthio)-6-methoxy-7-(trifluoromethanesulphonyloxy)quinazoline (1.0 g, 2.82 mmol) in dimethylformamide (30 ml) was reacted with propargyl alcohol (0.51 ml, 8.75 mmol) in the presence of bisdichloro(triphenylphosphine) palladium (100 mg, 0.14 mmol) copper (I) iodide (40 mg) and triethylamine (1.7 ml, 0.0124 mmol) at 90° C. for 2.5 hours under argon. The solvent was evaporated in vacuo, water and hydrochloric acid (2.0 N) were added, and the mixture was extracted with ethyl acetate. Purification by flash chromatography on silica gel, eluting with 7.5% methanol in dichloromethane, yielded 4-(methylthio)-6-methoxy-7-(3-hydroxyprop-1-ynyl)quinazoline (122 mg, 17% yield):

후처리

  1. customThe solvent was evaporated in vacuo, water and hydrochloric acid (2.0 N)
  2. additionwere added
  3. extractionthe mixture was extracted with ethyl acetate
  4. customPurification by flash chromatography on silica gel
  5. washeluting with 7.5% methanol in dichloromethane

출처 및 근거

ORD 기록
ord-42c6ac856b084e63aa63b595414e1d06
출처 데이터셋
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07709479B1

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