HCID 86647731, compound → HCID 59583362, compound
Reaction equation
C([O:5][C:6]([CH:8]([NH:35]C(=O)OC(C)(C)C)[CH2:9][O:10][P:11]([OH:34])(=[O:33])[O:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][NH:19][C:20](=[O:32])[CH2:21][CH2:22][CH:23]([P:28](=[O:31])([OH:30])[OH:29])[P:24]([OH:27])([OH:26])=[O:25])=[O:7])(C)(C)C>C(O)(C(F)(F)F)=O>[NH2:35][CH:8]([C:6]([OH:7])=[O:5])[CH2:9][O:10][P:11](=[O:33])([OH:34])[O:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][NH:19][C:20](=[O:32])[CH2:21][CH2:22][CH:23]([P:24]([OH:26])([OH:27])=[O:25])[P:28](=[O:29])([OH:30])[OH:31]Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
60 mg of 16-(tert-butoxycarbonyl)-13-hydroxy-20,20-dimethyl-13-oxido-4,18-dioxo-1-phosphono-12,14,19-trioxa-5,17-diaza-13-phosphahenicos-1-yl-phosphonic acid are stirred in 1 ml of TFA for 2 hours.
Sources & evidence
- ORD record
- ord-eb0f1a310b8e4092a03d4dfaf613c807
- Source dataset
- uspto-grants-2010_08
- Patent number
- US07780953B2
Reaction notes
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