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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789825Generated: October 27, 2026

1,2-Dichloroethane → 2-[N,N-bis(tert-butoxycarbonyl)amino]-5-(tert-butyl-dimethyl-silanyloxymethyl)-3-methylpyridin

https://huagongshe.com/reaction/1789825

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantDiethyl EtherHCID 3283—
ReactantPotassium FluorideHCID 522689—
ReactantTert-butyl-dimethyl-(tributylstannylmethoxy)silaneHCID 14270862—
Reactant2-(N,N-BisBOC-amino)-5-bromo-3-methylpyridineHCID 22036040—
CatalystHCID 178418476HCID 178418476—
Product2-[N,N-bis(tert-butoxycarbonyl)amino]-5-(tert-butyl-dimethyl-silanyloxymethyl)-3-methylpyridinHCID 13172582759%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 5-bromo-2-[N,N-bis(tert-butoxycarbonyl)amino]-3-methyl-pyridin (26.0 g, 67.1 mmol), tert-butyl-dimethyl-tributylstannanylmethoxy-silane (47.6 g, 109 mmol), and bis(triphenylphosphine)palladium(II) dichloride (0.90 g, 1.42 mmol) in 1,2-dichloroethane (80 mL) was stirred at 90° C. for two days. The mixture was cooled to 0° C. and diethyl ether (200 mL) was added followed by saturated aqueous potassium fluoride (40 mL). The mixture was stirred vigourously for 30 min and filtered. The organic phase was washed with water, dried and concentrated under reduced pressure. Flash chromatography (hexane/EtOAc, 100:0→95:5) gave 2-[N,N-bis(tert-butoxycarbonyl)amino]-5-(tert-butyl-dimethyl-silanyloxymethyl)-3-methylpyridin (18.0 g, 59%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07071175B1
Source datasetuspto-grants-2006_07
ORD IDord-36d991e903c24644903420e72332da4d
Source noteuspto-grants-2006_07