HCID 86641131, compound → HCID 86641130, compound
Reaction equation
[CH2:1]([O:3][P:4]([CH:9]=[CH:10][C:11]1([N:29]=[N+:30]=[N-:31])[CH:18]2[CH:14]([O:15]C(C)(C)[O:17]2)[CH:13]([N:21]2[CH:26]=[CH:25][C:24](=[O:27])[NH:23][C:22]2=[O:28])[O:12]1)(=[O:8])[O:5][CH2:6][CH3:7])[CH3:2]>C(O)=O.O>[CH2:1]([O:3][P:4]([CH:9]=[CH:10][C:11]1([N:29]=[N+:30]=[N-:31])[CH:18]([OH:17])[CH:14]([OH:15])[CH:13]([N:21]2[CH:26]=[CH:25][C:24](=[O:27])[NH:23][C:22]2=[O:28])[O:12]1)(=[O:8])[O:5][CH2:6][CH3:7])[CH3:2]Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
Compound 48.4 (130 mg, 0.29 mmol) was dissolved in 90% formic acid in water (2.8 mL). The solution was stirred at rt for 2 h and then concentrated under reduced pressure. The residue was used in the next step reaction without further purification.
Workup
- concentrationconcentrated under reduced pressure
- customThe residue was used in the next step reaction without further purification
Sources & evidence
- ORD record
- ord-93a5acaf10ba4204ab92db75bcaa26bb
- Source dataset
- uspto-grants-2012_12
- Patent number
- US08324179B2
Reaction notes
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