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Stannous Chloride → [3-(2-Pyridin-3-yl-1,3-thiazol-4-yl)phenyl]amine

HRID 1977751
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인쇄 미리보기

반응식

HRID 1977751 반응식
Br.[N+:2]([C:5]1[CH:6]=[C:7]([C:11]2[N:12]=[C:13]([C:16]3[CH:17]=[N:18][CH:19]=[CH:20][CH:21]=3)[S:14][CH:15]=2)[CH:8]=[CH:9][CH:10]=1)([O-])=O.[Sn](Cl)Cl>C(O)C.Cl>[NH2:2][C:5]1[CH:6]=[C:7]([C:11]2[N:12]=[C:13]([C:16]3[CH:17]=[N:18][CH:19]=[CH:20][CH:21]=3)[S:14][CH:15]=2)[CH:8]=[CH:9][CH:10]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 24479Stannous Chloride2회HCID 28238744-(3-Nitrophenyl)-2-(3-pyridyl)-thiazole hydrobromide

생성물 1

HCID 22724371[3-(2-Pyridin-3-yl-1,3-thiazol-4-yl)phenyl]amine수율 85%

시약·촉매·용매 2

HCID 313Hydrochloric Acid용매HCID 702Ethanol용매

반응 조건

온도
50 °C

실험 절차

A suspension of 4-(3-nitrophenyl)-2-(3-pyridyl)-thiazole hydrobromide (3.6 g, 10 mmol) in ethanol (150 ml) was treated with a solution of tin (II) chloride (3.7 g, 30 mmol) in concentrated hydrochloric acid (12 ml). The mixture was heated at 50° C. for 16 h. A further portion of tin (II) chloride (2.9 g, 15 mmol) was added and the mixture heated at 50° C. for a further 4 hours before being evaporated to dryness. The residue was partitioned between ethyl acetate and 1M aqueous sodium hydroxide. The ethyl acetate extract was dried (Na2SO4) and filtered through a plug of silica. Evaporation afforded the title compound as a yellow solid (2.15 g, 85%).

후처리

  1. temperaturethe mixture heated at 50° C. for a further 4 hours
  2. custombefore being evaporated to dryness
  3. customThe residue was partitioned between ethyl acetate and 1M aqueous sodium hydroxide
  4. extractionThe ethyl acetate extract
  5. dry with materialwas dried (Na2SO4)
  6. filtrationfiltered through a plug of silica
  7. customEvaporation

출처 및 근거

ORD 기록
ord-18c131c991234916bc219bb6208cbe10
출처 데이터셋
uspto-grants-2001_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06235758B1

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