HCID 86645222, compound → HCID 86645221, compound
Reaction equation
[CH2:1]([N:3]([CH2:24][CH3:25])[C:4](=[O:23])[CH:5]([CH2:20][C:21]#[CH:22])[C:6]([NH:8][S:9](/[CH:12]=[CH:13]/[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)(=[O:11])=[O:10])=[O:7])[CH3:2]>C(NC1C=CC=CC=1)C>[CH2:24]([N:3]([C:1]1[CH:21]=[CH:20][CH:5]=[CH:4][CH:2]=1)[C:4](=[O:23])[CH:5]([CH2:20][C:21]#[CH:22])[C:6]([NH:8][S:9](/[CH:12]=[CH:13]/[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)(=[O:10])=[O:11])=[O:7])[CH3:25]Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
In the same manner as in Example 1 (4), a crude product was obtained using the compound (1.04 g) obtained in Example 215 (2) and N-ethylaniline (430 μL). This was purified by silica gel column chromatography to give the title compound (95 mg) as a white powder.
Workup
- customThis was purified by silica gel column chromatography
Sources & evidence
- ORD record
- ord-36ed856b70e64024b38f655c8e111e41
- Source dataset
- uspto-grants-2013_06
- Patent number
- US08461209B2
Reaction notes
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