HCID 581988, compound → HCID 18008096, compound
Reaction equation
[N:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[NH:11][CH2:12][CH2:13][CH2:14][OH:15].Br[CH2:17][C:18]1[CH:27]=[CH:26][CH:25]=[C:24]([CH3:28])[C:19]=1[O:20][CH2:21][C:22]#[N:23]>>[CH3:17][C:18]1[CH:27]=[CH:26][CH:25]=[C:24]([CH2:28][O:15][CH2:14][CH2:13][CH2:12][NH:11][C:2]2[CH:3]=[CH:4][C:5]3[C:10](=[CH:9][CH:8]=[CH:7][CH:6]=3)[N:1]=2)[C:19]=1[O:20][CH2:21][C:22]#[N:23]Participants
3
Procedure
MS (ESI) 362 (M+H)+. Prepared from 3-(quinolin-2-ylamino)-propan-1-ol and (2-bromomethyl-6-methyl-phenoxy)-acetonitrile.
Sources & evidence
- ORD record
- ord-57bb269764e44a4baf4fd3bc47dd6a1c
- Source dataset
- uspto-grants-2008_10
- Patent number
- USRE040558E1
Reaction notes
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