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

HRID 1429662
ノート
印刷プレビュー

反応式

HRID 1429662 の反応式
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
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

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

生成物 1

HCID 598058596-(Trifluoromethyl)pyridazin-3-amine収率 93%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
100 °C

実験手順

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+)

後処理

  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

出典と根拠

ORDレコード
ord-7157ef4b97684c03a32b00946bae8736
出典データセット
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08940743B2

反応ノート

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