Reaction equation
CO[C:3]1[CH:4]=[C:5]([N:11]2[CH2:16][CH2:15][NH:14][C@H:13]([CH3:17])[CH2:12]2)[CH:6]=[CH:7][C:8]=1[O:9][CH3:10].Br[C:19]1C=CC2OCCC=2C=1>>[O:9]1[C:8]2[CH:7]=[CH:6][C:5]([N:11]3[CH2:16][CH2:15][NH:14][C@H:13]([CH3:17])[CH2:12]3)=[CH:4][C:3]=2[CH2:19][CH2:10]1Participants
3
Procedure
The title compound was prepared following the procedure of Intermediate 25, but starting from 5-bromo-2,3-dihydrobenzo[b]furan. Purification by flash chromatography (CHCl3/MeOH) gave the title compound as a brown oil. M+(ESI): 219.2. HPLC (Condition A), Rt: 1.3 min (HPLC purity: 99.9%).
Workup
- customThe title compound was prepared
- customPurification by flash chromatography (CHCl3/MeOH)
Sources & evidence
- ORD record
- ord-c5f72056f07d470da389ea08d9d675b5
- Source dataset
- uspto-grants-2012_08
- Patent number
- US08247437B2
Linked notes
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