Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Bromotrimethylsilane | HCID 76113 | — |
| Reactant | HCID 90370293 | HCID 90370293 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 90370288 | HCID 90370288 | 24.2% |
Reaction Steps
A mixture of 180 mg of 4-[2-(4-{[(2-{[3-({[4-(diethoxyphosphoryl)butanoyl](isopropyl)amino}methyl)benzoyl]amino}-4,5,6,7-tetrahydro-1-benzothiophen-3-yl)carbonyl]amino}phenyl)ethyl]benzoic acid, 0.040 mL of bromotrimethylsilane, and 3.6 mL of chloroform was stirred overnight at room temperature. Water was added to the reaction mixture, followed by extraction with chloroform. The organic layer was dried over anhydrous sodium sulfate, and the solvent was removed under reduced pressure. The residue was purified by silica gel column chromatography, thereby obtaining 42 mg of 4-(2-{4-[({2-[(3-{[{4-[ethoxy(hydroxy)phosphoryl]butanoyl}(isopropyl)amino]methyl}benzoyl)amino]-4,5,6,7-tetrahydro-1-benzothiophen-3-yl}carbonyl)amino]phenyl}ethyl)benzoic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09062032B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-f33228c00eb4460a8c221f1a01f74f26 |
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| Source note | uspto-grants-2015_06 |
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