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O-Xylene → 2-(2-Fluorophenyl)thiazolo[5,4-b]pyridine

HRID 259565
ノート
印刷プレビュー

反応式

HRID 259565 の反応式
[F:1][C:2]1[CH:17]=[CH:16][CH:15]=[CH:14][C:3]=1[C:4]([NH:6][C:7]1[C:8](=O)[NH:9][CH:10]=[CH:11][CH:12]=1)=O.C1(C)C(C)=CC=CC=1.P12(SP3(SP(SP(S3)(S1)=S)(=S)S2)=S)=[S:27]>N1C=CC=CC=1>[F:1][C:2]1[CH:17]=[CH:16][CH:15]=[CH:14][C:3]=1[C:4]1[S:27][C:8]2[C:7]([N:6]=1)=[CH:12][CH:11]=[CH:10][N:9]=2
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 3

HCID 7237O-XyleneHCID 14817Phosphorus sulfide (P2S5)HCID 124613983-(2-Fluorobenzoylamino)-2-pyridone

生成物 1

HCID 227547712-(2-Fluorophenyl)thiazolo[5,4-b]pyridine

試薬・触媒・溶媒 1

HCID 1049Pyridine溶媒

実験手順

3-(2-Fluorobenzoylamino)-2-pyridone (2 g.), 60 ml. of xylene and 15 ml of pyridine were heated until solution was complete. To this solution was added 6.5 grams of phosphorus pentasulfide and the mixture was heated at reflux for 16 hours. The reaction mixture was decanted from a gummy residue while hot, and the solvents were concentrated to dryness. The crystalline residue was recrystallized from ethanol to give 2-(2-fluorophenyl)thiazolo[ 5,4-b]pyridine, m.p. 119°-121° C.

後処理

  1. temperaturethe mixture was heated
  2. temperatureat reflux for 16 hours
  3. customThe reaction mixture was decanted from a gummy residue while hot, and the solvents
  4. concentrationwere concentrated to dryness
  5. customThe crystalline residue was recrystallized from ethanol

出典と根拠

ORDレコード
ord-f46c679bcfa345cb8ce39092c9cc91f3
出典データセット
uspto-grants-1977_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04038396

反応ノート

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