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Sulfur → Methyl 6-fluoroisoquinoline-3-carboxylate

HRID 340881
ノート
印刷プレビュー

反応式

HRID 340881 の反応式
[CH3:1][O:2][C:3]([CH:5]1[CH2:14][C:13]2[C:8](=[CH:9][CH:10]=[C:11]([F:15])[CH:12]=2)[CH2:7][NH:6]1)=[O:4].[S]>C1(C)C(C)=CC=CC=1>[CH3:1][O:2][C:3]([C:5]1[N:6]=[CH:7][C:8]2[C:13]([CH:14]=1)=[CH:12][C:11]([F:15])=[CH:10][CH:9]=2)=[O:4]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 5362487SulfurHCID 57947410Methyl 6-fluoro-1,2,3,4-tetrahydroisoquinoline-3-carboxylate

生成物 1

HCID 57947434Methyl 6-fluoroisoquinoline-3-carboxylate

試薬・触媒・溶媒 1

HCID 7237O-Xylene溶媒

反応条件

温度
150 °C

実験手順

A mixture of 6-fluoro-1,2,3,4-tetrahydro-isoquinoline-3-carboxylic acid methyl ester (92 g) and sulfur (42 g, 3 equiv.) in xylene (5 L) was stirred at 150° C. for 16 h. The reaction mixture was concentrated, and the resulting residue was dissolved in EtOAc, which was washed with water and brine, dried over Na2SO4, and concentrated under reduced pressure to give a crude mixture. Purification by flash column chromatography (hexanes/EtOAc, gradient 50%-100%) gave 6-fluoro-isoquinoline-3-carboxylic acid methyl ester as a light yellow solid (27 g, 24% for 3 steps). LRMS (M+H+) m/z 206.1.

後処理

  1. concentrationThe reaction mixture was concentrated
  2. dissolutionthe resulting residue was dissolved in EtOAc
  3. washwhich was washed with water and brine
  4. dry with materialdried over Na2SO4
  5. concentrationconcentrated under reduced pressure
  6. customto give a crude mixture
  7. customPurification by flash column chromatography (hexanes/EtOAc, gradient 50%-100%)

出典と根拠

ORDレコード
ord-9b06ac16b3574c96b85eff5292b92982
出典データセット
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08895582B2

反応ノート

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