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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | Tert-butyl-dimethyl-(tributylstannylmethoxy)silane | HCID 14270862 | — |
| Reactant | 2-(N,N-BisBOC-amino)-5-bromo-3-methylpyridine | HCID 22036040 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Product | 2-[N,N-bis(tert-butoxycarbonyl)amino]-5-(tert-butyl-dimethyl-silanyloxymethyl)-3-methylpyridin | HCID 131725827 | 59% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07071175B1 |
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| Source dataset | uspto-grants-2006_07 |
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| ORD ID | ord-36d991e903c24644903420e72332da4d |
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| Source note | uspto-grants-2006_07 |
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