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

HRID 2233266
ノート
印刷プレビュー

反応式

HRID 2233266 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

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

生成物 1

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

試薬・触媒・溶媒 2

HCID 8471Triethylamine触媒HCID 6228Dimethylformamide溶媒

実験手順

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):

後処理

  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

出典と根拠

ORDレコード
ord-42c6ac856b084e63aa63b595414e1d06
出典データセット
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07709479B1

反応ノート

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