3-Bromo-1-propanol → HCID 12021118, compound
Reaction equation
[Br:1][C:2]1[CH:3]=[CH:4][C:5]2[N:6]3[CH:19]=[C:18]([CH2:20][C:21]4[CH:22]=[N:23][CH:24]=[CH:25][CH:26]=4)[C:17](=[O:27])[C:8]4[CH:9]=[C:10]([OH:16])[CH:11]=[C:12]([S:13][C:14]=2[CH:15]=1)[C:7]3=4.Br[CH2:29][CH2:30][CH2:31][OH:32]>>[Br:1][C:2]1[CH:3]=[CH:4][C:5]2[N:6]3[CH:19]=[C:18]([CH2:20][C:21]4[CH:22]=[N:23][CH:24]=[CH:25][CH:26]=4)[C:17](=[O:27])[C:8]4[CH:9]=[C:10]([O:16][CH2:29][CH2:30][CH2:31][OH:32])[CH:11]=[C:12]([S:13][C:14]=2[CH:15]=1)[C:7]3=4Participants
3
Procedure
According to Example 34, the compound (120 mg) produced in Example 54 was reacted with 3-bromopropanol (0.04 mL) to obtain the title compound (72 mg; 53%).
Sources & evidence
- ORD record
- ord-22e25eb9db674e9488ca3324a22a359c
- Source dataset
- uspto-grants-2002_11
- Patent number
- US06476021B1
Reaction notes
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