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

HRID 1429662
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HRID 1429662 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-trifluoromethyl-pyridazine (1.6 g, 8.8 mmol) (prepared by a procedure similar to that described in Tetrahedron, 1999, 55 (52), 15067-15070) and ammonium hydroxide (30 ml) in THF (10 ml) was heated at 100° C. in a microwave reactor (Emrys Optimizer; 0-9 Barr) for 1 h. After this period, the reaction mixture was evaporated and the residue extracted with dichloromethane. The combined extracts were dried (MgSO4), filtered and the solvents evaporated in vacuo to give D6 (1.3 g, 93%). C5H4F3N3 requires 163; Found 164 (MH+)

후처리

  1. customprepared by a procedure similar to
  2. waitAfter this period
  3. customthe reaction mixture was evaporated
  4. extractionthe residue extracted with dichloromethane
  5. dry with materialThe combined extracts were dried (MgSO4)
  6. filtrationfiltered
  7. customthe solvents evaporated in vacuo

출처 및 근거

ORD 기록
ord-7157ef4b97684c03a32b00946bae8736
출처 데이터셋
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08940743B2

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