Iodoethane → HCID 57572007, compound
Reaction equation
[O:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[C:9]([C:10]3[CH:11]=[C:12]([N:16]4[C:20]5[CH:21]=[CH:22][C:23]([CH:25]([OH:27])[CH3:26])=[CH:24][C:19]=5[N:18]=[CH:17]4)[CH:13]=[CH:14][CH:15]=3)[C:4]=2[O:3][CH2:2]1.[H-].[Na+].[CH2:30](I)[CH3:31]>>[O:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[C:9]([C:10]3[CH:11]=[C:12]([N:16]4[C:20]5[CH:21]=[CH:22][C:23]([CH:25]([O:27][CH2:30][CH3:31])[CH3:26])=[CH:24][C:19]=5[N:18]=[CH:17]4)[CH:13]=[CH:14][CH:15]=3)[C:4]=2[O:3][CH2:2]1Participants
4
Procedure
This was prepared from compound 17 by deprotonisation with sodium hydride followed by alkylation with ethyliodide using standard conditions. LC-ESI-HRMS of [M+H]+ shows 387.1705 Da. Calc. 387.170868 Da, dev. −1 ppm
Sources & evidence
- ORD record
- ord-4a9c51da4b934000b2eb392f396a9e61
- Source dataset
- uspto-grants-2012_10
- Patent number
- US08288418B2
Reaction notes
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