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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2361630Generated: November 1, 2026

Sodium methanolate methanol → HCID 86712034, compound

https://huagongshe.com/reaction/2361630

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium methanolate methanolHCID 23694274—
ReactantHCID 86712035HCID 86712035—
SolventMethanolHCID 887—
ProductHCID 86712034HCID 86712034—

Reaction Conditions

Temperature0 °C

Reaction Steps

250 mg (0.45 mmol) of the above product 6 as the starting material is dissolved in 15 mL of MeOH and cooled to 0° C. Then 5 mL of 0.01N NaOMe/MeOH is added with continuously stirring. After the starting material completely disappears, a cationic exchange resin (Dowex 500 WX8-400, H+form) is used to neutralize. After filtration, the solution is concentrated at reduced pressure at 30° C. to obtain a product (1-(β-D-arabinofuranosyl)-5-trimethylstannylpyrimidin-2,4(3H)-dione) 7. Its weight and yield are 140 mg and 80% respectively.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691789B2
Source datasetuspto-grants-2014_04
ORD IDord-fbf09fbacf094ac98b8ff428d2810e7b
Source noteuspto-grants-2014_04