Hydrogen Bromide → HCID 19595243, compound
Reaction equation
C[O:2][C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][CH:11]=1)[CH2:8][N:7]([NH:12][C:13]1[CH:18]=[CH:17][N:16]=[CH:15][CH:14]=1)[CH2:6]2.[BrH:19]>>[BrH:19].[N:16]1[CH:15]=[CH:14][C:13]([NH:12][N:7]2[CH2:6][C:5]3[C:9](=[CH:10][CH:11]=[C:3]([OH:2])[CH:4]=3)[CH2:8]2)=[CH:18][CH:17]=1Participants
3
Conditions
- Temperature
- 10 °C
Procedure
A solution of 2,3-dihydro-5-methoxy-N-(4-pyridinyl)-1 H-isoindol-2-amine (5.25 g) in 48% hydrobromic acid (35 ml) was heated under reflux for 5 hrs, with stirring. The reaction mixture was cooled to about 10° C. and filtered. The filter cake was washed with cold water and dried under vacuum in an oven at 80° C. to give 4.8 g (72%) of product. The product was recrystallized from water and dried under vacuum at 80° C. to give 3.1 g (46%) of the analytical sample, mp 261-264° C.
Workup
- temperatureunder reflux for 5 hrs
- filtrationfiltered
- washThe filter cake was washed with cold water
- customdried under vacuum in an oven at 80° C.
Sources & evidence
- ORD record
- ord-cc0cb014f334449f9c9748620d748bf2
- Source dataset
- uspto-grants-1999_12
- Patent number
- US06004977
Reaction notes
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