Water → HCID 19857817, compound
Reaction equation
[C:1]1(=O)[N:6]([CH2:7][CH2:8][CH2:9][N:10]2[C:18]3=[N:19][C:20]4[C:25]([N:26]=[C:17]3[C:16]3[CH:15]=[CH:14][CH:13]=[CH:12][C:11]2=3)=[CH:24][CH:23]=[CH:22][CH:21]=4)[C:5](=O)[CH2:4][CH2:3][CH2:2]1.[Li].O>O1CCCC1>[N:6]1([CH2:7][CH2:8][CH2:9][N:10]2[C:18]3=[N:19][C:20]4[C:25]([N:26]=[C:17]3[C:16]3[CH:15]=[CH:14][CH:13]=[CH:12][C:11]2=3)=[CH:24][CH:23]=[CH:22][CH:21]=4)[CH2:1][CH2:2][CH2:3][CH2:4][CH2:5]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
6-(3-glutarimidopropyl)-6H-indolo(2,3-b)quinoxaline (3.72 g) is heated under reflux with lithium aluminumhydride (0.80 g) in tetrahydrofuran (40 ml) for 6 hours, and then water (2 ml) is dropped thereto carefully. After stirring for 1 hour solid material is separated away and the residue is concentrated. The residue is dissolved in dry ether and the base is precipitated as hydrochloride by addition of hydrogen chloride. Yield: 2.60 g (68%), mp. 262°-266° C.
Workup
- customis separated away
- concentrationthe residue is concentrated
- dissolutionThe residue is dissolved in dry ether
- customthe base is precipitated as hydrochloride by addition of hydrogen chloride
Sources & evidence
- ORD record
- ord-bb459292d6b844f7be3d1e202e8fe97b
- Source dataset
- uspto-grants-1990_04
- Patent number
- US04916124
Reaction notes
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