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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2262401Generated: November 1, 2026

Toluene → HCID 86761231, compound

https://huagongshe.com/reaction/2262401

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantHCID 86761226HCID 86761226—
ReactantHCID 131728575HCID 131728575—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86761231HCID 8676123180.4%

Reaction Steps

The above-obtained 3′,5′-bis-O-(tert-butyldimethylsilyl)-6-O-diphenylcarbamoyl-2-N-methylthiocarbamoyldeoxyguanosine (900 mg, 1.17 mmol) was azeotroped with anhydrous tetrahydrofuran three times and dissolved in anhydrous tetrahydrofuran (6.0 mL), and triethylamine 3 hydrogen fluoride (574 μL, 3.51 mmol) was added thereto. The mixture was stirred at room temperature overnight, and then toluene (5 mL) was added thereto. The solvent was evaporated under reduced pressure. To the residue, methanol (5 mL) and hexane (25 mL) were added for precipitation. The resulting precipitate was purified by filtration to give 6-O-diphenylcarbamoyl-2-N-methylthiocarbamoyldeoxyguanosine (504 mg, 80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07851157B1
Source datasetuspto-grants-2010_12
ORD IDord-8c7eacf5367f4e24b5a7151454483938
Source noteuspto-grants-2010_12