HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1348578Generated: November 3, 2026
Water → (1S)-5-(1-Methyl-6-oxo-4-pyridin-4-yl-1,6-dihydro-pyrimidin-2-yl)-2,5-diaza-bicyclo[2.2.1]heptane-2-carboxylic acid tert-butyl ester
https://huagongshe.com/reaction/1348578
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-chloro-3-methyl-6-pyridin-4-yl-3H-pyrimidin-4-one hydrochloride | HCID 23024527 | — |
| Reactant | (1S,4S)-(-)-2-Boc-2,5-diazabicyclo[2.2.1]heptane | HCID 66592084 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (1S)-5-(1-Methyl-6-oxo-4-pyridin-4-yl-1,6-dihydro-pyrimidin-2-yl)-2,5-diaza-bicyclo[2.2.1]heptane-2-carboxylic acid tert-butyl ester | HCID 68801880 | 72.1% |
Reaction Steps
A mixture containing 10.7 ml (78.14 mmol) of triethylamine, 13.6 g (52.7 mmol) of 2-chloro-3-methyl-6-pyridin-4-yl-3H-pyrimidin-4-one hydrochloride (1:1), 6.0 g (30.24 mmol) of (1S)-2,5-diaza-bicyclo[2.2.1]heptane-2-carboxylic acid tert-butyl ester in 500 ml of anhydrous dimethylformamide is stirred at 20° C. for 6 h. Water is added to the cooled mixture and the resulting solution extracted with ethyl acetate. The combined extracts are washed with saturated aqueous ammonium chloride and saturated aqueous sodium chloride then-evaporated. The crude product is refluxed in diethylether for 1 h to afford 8.36 g of pure product as a brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07211581B2 |
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| Source dataset | uspto-grants-2007_05 |
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| ORD ID | ord-0c65aa05e37f49ecb6cd4748622a6d81 |
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| Source note | uspto-grants-2007_05 |
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