Ethylamine hydrochloride → HCID 22981224, compound
Reaction equation
[C:1]([O:5][C:6]([N:8]([C:20]([O:22][C:23]([CH3:26])([CH3:25])[CH3:24])=[O:21])[CH2:9][C:10]1[CH:15]=[C:14]([N+:16]([O-:18])=[O:17])[CH:13]=[CH:12][C:11]=1F)=[O:7])([CH3:4])([CH3:3])[CH3:2].Cl.[CH2:28]([NH2:30])[CH3:29]>>[C:1]([O:5][C:6]([N:8]([C:20]([O:22][C:23]([CH3:26])([CH3:25])[CH3:24])=[O:21])[CH2:9][C:10]1[CH:15]=[C:14]([N+:16]([O-:18])=[O:17])[CH:13]=[CH:12][C:11]=1[NH:30][CH2:28][CH3:29])=[O:7])([CH3:4])([CH3:3])[CH3:2]Participants
3
Procedure
Using the compound obtained in Example 263 as a starting material and also using ethylamine hydrochloride as a reagent, the same procedure of Example 264 gave the titled compound (yield, 52%).
Sources & evidence
- ORD record
- ord-530ba8d240f1487ca555fbf21a16283a
- Source dataset
- uspto-grants-2003_03
- Patent number
- US06534546B1
Reaction notes
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