Ammonia → HCID 59691680, compound
Reaction equation
[CH2:1]([N:3]([CH2:20][CH3:21])[CH2:4][CH2:5][O:6][C:7]1[CH:12]=[CH:11][C:10]([NH:13]C(=O)C)=[CH:9][C:8]=1[N+:17]([O-:19])=[O:18])[CH3:2].Cl.N>>[CH2:20]([N:3]([CH2:1][CH3:2])[CH2:4][CH2:5][O:6][C:7]1[CH:12]=[CH:11][C:10]([NH2:13])=[CH:9][C:8]=1[N+:17]([O-:19])=[O:18])[CH3:21]Participants
4
Procedure
A solution of 1.85 g (6.264 mmol) N-[4-(2-diethylamino-ethoxy)-3-nitro-phenyl]-acetamide (Z31a) in semiconc. aqueous HCl was stirred for 2 h at 100° C., cooled to RT, made basic with ice and conc. aqueous ammonia and the aqueous phase was exhaustively extracted with EtOAc. The combined org. phases were washed with water and dried over sodium sulphate.
Workup
- extractionthe aqueous phase was exhaustively extracted with EtOAc
- washphases were washed with water
- dry with materialdried over sodium sulphate
Sources & evidence
- ORD record
- ord-c2bf1d3411e1473d8f9f5c1b9f5027db
- Source dataset
- uspto-grants-2008_04
- Patent number
- US07351719B2
Reaction notes
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