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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2079491Generated: November 2, 2026

Sodium Thiosulfate → Briciclib

https://huagongshe.com/reaction/2079491

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
ReactantBromotrimethylsilaneHCID 76113—
ReactantSodiumHCID 5360545—
Reactant5-((2,4,6-Trimethoxystyrylsulfonyl)methyl)-2-methoxy-phenyl dibenzyl phosphateHCID 72959905—
SolventDichloromethaneHCID 6344—
ProductBriciclibHCID 1124849044%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932242B2
Source datasetuspto-grants-2011_04
ORD IDord-1e0611e987e04a96909a37a01d6789c5
Source noteuspto-grants-2011_04