Hydrochloric Acid → HCID 20536091, compound
Reaction equation
[C:1]([C:3]1[C:4](=[O:26])[N:5]([CH2:24][CH3:25])[C:6](=[O:23])[C:7](=NC2C=CC(N(CC)CCO)=CC=2)[C:8]=1[CH3:9])#[N:2].Cl.[OH2:28]>>[C:1]([C:3]1[C:4](=[O:26])[N:5]([CH2:24][CH3:25])[C:6](=[O:23])[C:7](=[O:28])[C:8]=1[CH3:9])#[N:2]Participants
4
Procedure
1.02 g of 3-Cyano-1-ethyl-4-methyl-5-[4-(N-ethyl-N-hydroxyethylamino)phenylimino]-pyridine-2,6-dione (prepared as described in German Offenlegungsschrift No. 2808825) is stirred in 7 ml of water, and concentrated hydrochloric acid is slowly added until the blue dye had disappeared. A pale yellow solid precipitates, and is filtered off and recrystallised from ethyl acetate/petrol, yield 0.32 g, m.p. 159°-160° C. This is the compound of formula (4).
Workup
- customA pale yellow solid precipitates
- filtrationis filtered off
- customrecrystallised from ethyl acetate/petrol, yield 0.32 g, m.p. 159°-160° C
Sources & evidence
- ORD record
- ord-7c6220ac33b64113baa51ae73061ed26
- Source dataset
- uspto-grants-1982_06
- Patent number
- US04335245
Reaction notes
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