2-(Bromomethyl)benzonitrile → HCID 10291157, compound
Reaction equation
[CH3:1][C:2]1[CH:11]=[C:10]([N:12]2[CH2:16][CH2:15][CH2:14][CH2:13]2)[C:9]2[C:4](=[CH:5][C:6]([OH:17])=[CH:7][CH:8]=2)[N:3]=1.Br[CH2:19][C:20]1[CH:27]=[CH:26][CH:25]=[CH:24][C:21]=1[C:22]#[N:23]>>[CH3:1][C:2]1[CH:11]=[C:10]([N:12]2[CH2:16][CH2:15][CH2:14][CH2:13]2)[C:9]2[C:4](=[CH:5][C:6]([O:17][CH2:19][C:20]3[CH:27]=[CH:26][CH:25]=[CH:24][C:21]=3[C:22]#[N:23])=[CH:7][CH:8]=2)[N:3]=1Participants
3
Procedure
In analogy to example 6 there was prepared: on reaction of 2-methyl-4-pyrrolidin-1-yl-quinolin-7-ol with 2-bromomethyl benzonitrile, whereby the product was isolated as free base, 2-(2-methyl-4-pyrrolidin-1-yl-quinolin-7-yloxymethyl)-benzonitrile as a brown solid. ISP mass spectrum, m/e: 344.4 (M+1 calculated for C22H21N3O: 344).
Workup
- customIn analogy to example 6 there was prepared
Sources & evidence
- ORD record
- ord-2d6872f4b914458f9ff4eab9425e60d0
- Source dataset
- uspto-grants-2004_11
- Patent number
- US06818767B2
Reaction notes
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