Hydrogen iodide → HCID 136377642, compound
Reaction equation
C[O:2][C:3]1[CH:12]=[C:11]2[C:6]([C:7]([C:19]([OH:21])=[O:20])=[CH:8][C:9]([C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)=[N:10]2)=[CH:5][CH:4]=1.[IH:22]>>[IH:22].[OH:2][C:3]1[CH:12]=[C:11]2[C:6]([C:7]([C:19]([OH:21])=[O:20])=[CH:8][C:9]([C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)=[N:10]2)=[CH:5][CH:4]=1Participants
3
Procedure
1.5 g (5.4 mmol) of 7-methoxy-2-phenylquinoline-4-carboxylic acid were, added portionwise to 50 ml of 57% aqueous HI. The reaction mixture was refluxed and vigourously stirred for 5 hours; then it was evaporated in-vacuo to dryness to yield 2.1 g of the title compound.
Workup
- temperatureThe reaction mixture was refluxed
- customthen it was evaporated in-vacuo to dryness
Sources & evidence
- ORD record
- ord-e7395d36d43f49cfb9c68f252c24a541
- Source dataset
- uspto-grants-2009_01
- Patent number
- US07482458B2
Reaction notes
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