HCID 57779641, compound → HCID 57779539, compound
Reaction equation
[NH2:1][C:2]1[CH:7]=[C:6]([C:8]2[S:9][CH:10]=[CH:11][CH:12]=2)[CH:5]=[CH:4][C:3]=1[NH:13][C:14](=O)[CH:15]([C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1)[C:16]([O:18][CH2:19][C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)=[O:17]>CC(O)=O>[C:26]1([CH:15]([C:14]2[NH:1][C:2]3[CH:7]=[C:6]([C:8]4[S:9][CH:10]=[CH:11][CH:12]=4)[CH:5]=[CH:4][C:3]=3[N:13]=2)[C:16]([O:18][CH2:19][C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)=[O:17])[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 100 °C
Procedure
AcOH (3 mL) was added to compound 32 (463 mg, 1.04 mmol) and the reaction heated at 100° C. for 30 min. The solvent was evaporated under reduced pressure.
Workup
- customThe solvent was evaporated under reduced pressure
Sources & evidence
- ORD record
- ord-16aa53b1c00948df8714fcc6a04a91d8
- Source dataset
- uspto-grants-2015_08
- Patent number
- US09096565B2
Reaction notes
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