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

HRID 259565
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인쇄 미리보기

반응식

HRID 259565 반응식
[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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

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

생성물 1

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

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-f46c679bcfa345cb8ce39092c9cc91f3
출처 데이터셋
uspto-grants-1977_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04038396

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