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Ammonium Hydroxide → 6-(Trifluoromethyl)pyridazin-3-amine

HRID 1412037
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HRID 1412037 반응식
Cl[C:2]1[N:3]=[N:4][C:5]([C:8]([F:11])([F:10])[F:9])=[CH:6][CH:7]=1.[OH-].[NH4+:13]>C1COCC1>[F:9][C:8]([F:11])([F:10])[C:5]1[N:4]=[N:3][C:2]([NH2:13])=[CH:7][CH:6]=1
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참가 물질

4

반응물 2

HCID 14923Ammonium HydroxideHCID 282425263-Chloro-6-(trifluoromethyl)pyridazine

생성물 1

HCID 598058596-(Trifluoromethyl)pyridazin-3-amine수율 93%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
100 °C

실험 절차

A mixture of 3-chloro-6-trifluoromethylpyridazine (1.6 g, 8.80 mmol) and ammonium hydroxide (9 mL) in THF (3 mL) was heated at 100° C. in a microwave reactor for 1 h. After this period, the reaction mixture was evaporated and the residue was extracted with dichloromethane. The combined extract was dried over with MgSO4, filtered, and evaporated under reduce pressure to afford 301a (1.3 g, 93%) as a white solid. MS-ESI: [M+H]+ 164.1

후처리

  1. waitAfter this period
  2. customthe reaction mixture was evaporated
  3. extractionthe residue was extracted with dichloromethane
  4. extractionThe combined extract
  5. dry with materialwas dried over with MgSO4
  6. filtrationfiltered
  7. customevaporated

출처 및 근거

ORD 기록
ord-9e9fdb0f450b452a90aeaae5586db777
출처 데이터셋
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08921353B2

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