3-Bromo-1-propanol → HCID 86755601, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([C:11]2[C@H:20]3[C@H:15]([CH2:16][CH2:17][CH2:18][CH2:19]3)[C:14](=[O:21])[NH:13][N:12]=2)[CH:6]=[CH:7][C:8]=1[O:9][CH3:10].Br[CH2:23][CH2:24][CH2:25][OH:26].COC1C=C(C2[C@H]3[C@H](CCCC3)C(=O)N(C)N=2)C=CC=1OC>>[OH:26][CH2:25][CH2:24][CH2:23][N:13]1[N:12]=[C:11]([C:5]2[CH:6]=[CH:7][C:8]([O:9][CH3:10])=[C:3]([O:2][CH3:1])[CH:4]=2)[C@H:20]2[C@H:15]([CH2:16][CH2:17][CH2:18][CH2:19]2)[C:14]1=[O:21]Participants
4
Procedure
Prepared from compound 1 and 3-bromo-1-propanol as described for compound 8. Purified by chromatography (dichloromethane). Crystallized from diethyl ether/petroleum ether (60-95° C.). M.p. 94-97° C.
Workup
- customPurified by chromatography (dichloromethane)
- customCrystallized from diethyl ether/petroleum ether (60-95° C.)
Sources & evidence
- ORD record
- ord-2e4d4b3e5f0a46df9808296b55ab96f3
- Source dataset
- uspto-grants-2000_08
- Patent number
- US06103718
Reaction notes
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