Ammonia → 3-Chloroquinoxalin-2-amine
Reaction equation
[Cl:1][C:2]1[C:11](Cl)=[N:10][C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[N:3]=1.[NH3:13]>>[NH2:13][C:11]1[C:2]([Cl:1])=[N:3][C:4]2[C:9](=[CH:8][CH:7]=[CH:6][CH:5]=2)[N:10]=1Participants
3
Procedure
2.1 g (10.4 mmol) of 2,3-dichloroquinoxaline are stirred for 8 hours with 50 ml of 20% ethanolic ammonia in an autoclave at 80°–85° C. and autogenous pressure. The reaction solution is evaporated to dryness in a rotary evaporator, and the crude product is chromatographed over silica gel using toluene/ethyl acetate. The product-containing fractions are collected and evaporated in a rotary evaporator. Yield: 1.18 g (63%)
Workup
- customThe reaction solution is evaporated to dryness in a rotary evaporator
- customthe crude product is chromatographed over silica gel
- customThe product-containing fractions are collected
- customevaporated in a rotary evaporator
Sources & evidence
- ORD record
- ord-e554a052c4ba4202a78802598237d28d
- Source dataset
- uspto-grants-2006_09
- Patent number
- US07101537B2
Reaction notes
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