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

HRID 66377
ノート
印刷プレビュー

反応式

HRID 66377 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.

このページの内容参加物実験手順後処理出典と根拠反応ノート

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-d38a1cfacb134b248128f28d66a3c836
出典データセット
uspto-grants-1978_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04131677

反応ノート

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