HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1368261Generated: October 29, 2026
Water → tert-Butyl 5,6-dichloropyridin-3-ylcarbamate
https://huagongshe.com/reaction/1368261
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 5,6-Dichloronicotinic acid | HCID 247987 | — |
| Product | tert-Butyl 5,6-dichloropyridin-3-ylcarbamate | HCID 22485189 | — |
Reaction Steps
To a suspension of 5,6-dichloronicotinic acid (5.1 g) in tert-butyl alcohol (50 ml) were added triethylamine (2.7 g) and phosphorus diphenylazide (7.3 g) in a nitrogen atmosphere and the mixture was heated to 80° C. After 8 hr, the reaction mixture was cooled and water and ethyl acetate were added. The mixture was washed 3 times with water, saturated aqueous sodium hydrogen carbonate solution and saturated brine. The organic layer was dried over anhydrous magnesium sulfate, and the filtrate was concentrated. The residue was applied to flash silica gel chromatography (silica gel, 30 ml) and eluted with hexane:ethyl acetate=5:1-2:1 to give 3-(N-(tert-butoxycarbonyl)amino)-5,6-dichloropyridine as a colorless solid (6.49 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06573274B1 |
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| Source dataset | uspto-grants-2003_06 |
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| ORD ID | ord-b1ed9aa2d2854974aba022d522024587 |
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| Source note | uspto-grants-2003_06 |
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