Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | Bromotrimethylsilane | HCID 76113 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 5-((2,4,6-Trimethoxystyrylsulfonyl)methyl)-2-methoxy-phenyl dibenzyl phosphate | HCID 72959905 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Briciclib | HCID 11248490 | 44% |
Reaction Steps
To a stirred solution of 5-((2,4,6-trimethoxystyrylsulfonyl)methyl)-2-methoxy-phenyl dibenzyl phosphate (4.36 g, 6.7 mmol) in anhydrous DCM (40 mL) under nitrogen at 0° C. was added bromotrimethylsilane (2.14 g, 2.1 eq). The resulting mixture was stirred for 45 minutes and monitored by TLC. sodium When the reaction was complete, aqueous sodium thiosulfate (1%, 50 mL) was added and the resulting mixture was stirred for an additional 5 minutes. The organic phase was separated and the aqueous phase was extracted with ethyl acetate (3×25 mL). The combined organic extract was concentrated in vacuo to afford the crude 5-((2,4,6-trimethoxystyrylsulfonyl)methyl)-2-methoxyphenyl dihydrogen phosphate. The product was purified column chromatography on silica eluted with a methanol/chloroform gradient to yield 1.4 g of the purified product having a melting point of 202-205° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07932242B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-1e0611e987e04a96909a37a01d6789c5 |
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| Source note | uspto-grants-2011_04 |
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