Nebivolol → HCID 9933004, compound
Reaction equation
[CH:1]1[C:6]([F:7])=[CH:5][C:4]2[CH2:8][CH2:9][CH:10]([CH:12]([OH:29])[CH2:13][NH:14][CH2:15][CH:16]([OH:28])[CH:17]3[O:26][C:25]4[CH:24]=[CH:23][C:22]([F:27])=[CH:21][C:20]=4[CH2:19][CH2:18]3)[O:11][C:3]=2[CH:2]=1.[ClH:30].Cl>>[CH:23]1[C:22]([F:27])=[CH:21][C:20]2[CH2:19][CH2:18][CH:17]([CH:16]([OH:28])[CH2:15][NH:14][CH2:13][CH:12]([OH:29])[CH:10]3[O:11][C:3]4[CH:2]=[CH:1][C:6]([F:7])=[CH:5][C:4]=4[CH2:8][CH2:9]3)[O:26][C:25]=2[CH:24]=1.[ClH:30]Participants
3
Procedure
In a preferred embodiment the said form is obtained by conventional spray drying technique using a LabPlant SPD-005® spray drier. Nebivolol hydrochloride is dissolved in alcohol such as methanol under heating to obtain a clear solution or adjust pH below 2.0 of nebivolol base solution/suspension in alcohol using aqueous HCl/Alcoholic HCl/HCl gas, which is then spray dried for a period of 2 to 5 hours, and further isolating nebivolol hydrochloride Form T1.
Workup
- customIn a preferred embodiment the said form is obtained by conventional spray
- customdrying technique
- dissolutionNebivolol hydrochloride is dissolved in alcohol such as methanol
- temperatureunder heating
- customto obtain a clear solution
- customis then spray dried for a period of 2 to 5 hours
Sources & evidence
- ORD record
- ord-1f99891c7b164bd8893188ba6b3c37f3
- Source dataset
- uspto-grants-2014_01
- Patent number
- US08633241B2
Reaction notes
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