Isopropanol hydrochloride → 1218764-02-3
Reaction equation
[F:1][C:2]([F:23])([F:22])[C:3]1[CH:4]=[C:5]([N:13](C)[C:14](=O)OC(C)(C)C)[CH:6]=[C:7]([C:9]([F:12])([F:11])[F:10])[CH:8]=1.[ClH:24].CC(O)C>>[ClH:24].[CH3:14][NH:13][C:5]1[CH:6]=[C:7]([C:9]([F:10])([F:11])[F:12])[CH:8]=[C:3]([C:2]([F:1])([F:22])[F:23])[CH:4]=1Participants
3
Conditions
- Temperature
- 50 °C
Procedure
To the compound (12.4 g) obtained in step 2 was added 2N hydrogen chloride/2-propanol (100 mL), and the mixture was stirred at 50° C. for 2 hr. The reaction mixture was concentrated under reduced pressure to give the title compound (9.36 g, 93%) as a white powder.
Workup
- concentrationThe reaction mixture was concentrated under reduced pressure
Sources & evidence
- ORD record
- ord-00db87f2bb534e219705fd03a03b16a4
- Source dataset
- uspto-grants-2013_11
- Patent number
- US08592454B2
Reaction notes
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