Boron tribromide → 3-[1-(5-Fluoro-2-hydroxyphenyl)cycloprop-1-yl]-1-(2-(hydroxymethyl)quinolin-5-ylamino)-2-(trifluoromethyl)propan-2-ol
Reaction equation
[F:1][C:2]1[CH:3]=[CH:4][C:5]([O:32]C)=[C:6]([C:8]2([CH2:11][C:12]([C:28]([F:31])([F:30])[F:29])([OH:27])[CH2:13][NH:14][C:15]3[CH:24]=[CH:23][CH:22]=[C:21]4[C:16]=3[CH:17]=[CH:18][C:19]([CH2:25][OH:26])=[N:20]4)[CH2:10][CH2:9]2)[CH:7]=1.B(Br)(Br)Br>>[F:1][C:2]1[CH:3]=[CH:4][C:5]([OH:32])=[C:6]([C:8]2([CH2:11][C:12]([C:28]([F:29])([F:30])[F:31])([OH:27])[CH2:13][NH:14][C:15]3[CH:24]=[CH:23][CH:22]=[C:21]4[C:16]=3[CH:17]=[CH:18][C:19]([CH2:25][OH:26])=[N:20]4)[CH2:10][CH2:9]2)[CH:7]=1Participants
3
Reactant 2
Product 1
Procedure
Analogously to Example 38, 100 mg (0.22 mmol) of 3-[1-(5-fluoro-2-methoxyphenyl)cycloprop-1-yl]-1-(2-(hydroxymethyl)quinolin-5-ylamino)-2-(trifluoromethyl)propan-2-ol is reacted with 4.40 ml (4.40 mmol) of a 1 M boron tribromide solution. After working-up and purification on silica gel with hexane-ethyl acetate (0–100%) as well as with ethyl acetate-methanol (0–20%), 50 mg (50% of theory) of the product is obtained.
Workup
- custompurification on silica gel with hexane-ethyl acetate (0–100%) as well as with ethyl acetate-methanol (0–20%), 50 mg (50% of theory) of the product
- customis obtained
Sources & evidence
- ORD record
- ord-739048dbd83b4cd4b8934373fb846d02
- Source dataset
- uspto-grants-2006_09
- Patent number
- US07109212B2
Reaction notes
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