Hydrochloric Acid → HCID 21253084, compound
Reaction equation
C([N:4]1[CH2:13][CH2:12][C:11]2[C:6](=[C:7]([NH:18]C(=O)C)[C:8]([N+:15]([O-:17])=[O:16])=[CH:9][C:10]=2[Br:14])[CH2:5]1)(=O)C.[ClH:22]>>[ClH:22].[Br:14][C:10]1[CH:9]=[C:8]([N+:15]([O-:17])=[O:16])[C:7]([NH2:18])=[C:6]2[C:11]=1[CH2:12][CH2:13][NH:4][CH2:5]2Participants
3
Procedure
A solution of the product from Example 4 (11.7 g, 32.8 mmol) and 3N HCl (400 mL) was heated to reflux for 4 hours. Upon cooling to room temperature, the solids were filtered, washed with 3N HCl and diethyl ether, and air dried to give the title compound (7.8 g, 77% yield) as a yellow solid, mp-305-307° C.
Workup
- temperatureto reflux for 4 hours
- filtrationthe solids were filtered
- washwashed with 3N HCl and diethyl ether, and air
- customdried
Sources & evidence
- ORD record
- ord-cdfbd31871e6432ba358e67e2df908c3
- Source dataset
- uspto-grants-2000_05
- Patent number
- US06057313
Reaction notes
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