Tert-butyl 2-oxo-1,2,7,8-tetrahydro-1,6-naphthyridine-6(5h)-carboxylate
- Product Name
- Tert-butyl 2-oxo-1,2,7,8-tetrahydro-1,6-naphthyridine-6(5h)-carboxylate
- CAS No.
- 1036381-91-5
- Chemical Name
- Tert-butyl 2-oxo-1,2,7,8-tetrahydro-1,6-naphthyridine-6(5h)-carboxylate
- Synonyms
- 6-Boc-5,6,7,8-tetrahydro-1,6-naphthyridin-2(1H)-one;tert-butyl 2-oxo-1,2,7,8-tetrahydro-1,6-naphthyridine-6(5H)-...;tert-butyl 2-hydroxy-7,8-dihydro-1,6-naphthyridine-6(5H)-carboxylate;Tert-butyl 2-oxo-1,2,7,8-tetrahydro-1,6-naphthyridine-6(5h)-carboxylate;1,6-Naphthyridine-6(2H)-carboxylic acid, 1,5,7,8-tetrahydro-2-oxo-, 1,1-dimethylethyl ester
- CBNumber
- CB22657042
- Molecular Formula
- C13H18N2O3
- Formula Weight
- 250.29
- MOL File
- 1036381-91-5.mol
Tert-butyl 2-oxo-1,2,7,8-tetrahydro-1,6-naphthyridine-6(5h)-carboxylate Property
- Boiling point:
- 470.9±45.0 °C(Predicted)
- Density
- 1.20±0.1 g/cm3(Predicted)
- storage temp.
- 2-8°C
- pka
- 12.39±0.20(Predicted)
- Appearance
- White to off-white Solid
N-Bromosuccinimide Price
- Product number
- A660000
- Product name
- tert-Butyl2-oxo-1,2,7,8-tetrahydro-1,6-naphthyridine-6(5H)-carboxylate
- Purity
- 97%
- Packaging
- 100mg
- Price
- $198
- Updated
- 2021/12/16
- Product number
- A660000
- Product name
- tert-Butyl2-oxo-1,2,7,8-tetrahydro-1,6-naphthyridine-6(5H)-carboxylate
- Purity
- 97%
- Packaging
- 250mg
- Price
- $307
- Updated
- 2021/12/16
- Product number
- 1036381915
- Product name
- tert-Butyl2-oxo-1,2,7,8-tetrahydro-1,6-naphthyridine-6(5H)-carboxylate
- Packaging
- 1g
- Price
- $657.14
- Updated
- 2021/12/16
- Product number
- CD11361947
- Product name
- tert-Butyl2-oxo-1,2,7,8-tetrahydro-1,6-naphthyridine-6(5H)-carboxylate
- Purity
- 97%
- Packaging
- 1g
- Price
- $663
- Updated
- 2021/12/16
- Product number
- A660000
- Product name
- tert-Butyl2-oxo-1,2,7,8-tetrahydro-1,6-naphthyridine-6(5H)-carboxylate
- Purity
- 97%
- Packaging
- 1g
- Price
- $731
- Updated
- 2021/12/16
Tert-butyl 2-oxo-1,2,7,8-tetrahydro-1,6-naphthyridine-6(5h)-carboxylate Chemical Properties,Usage,Production
Synthesis
7341-96-0
79099-07-3
1036381-91-5
To a stirred solution of N-Boc-4-piperidone (35.6 g, 178.89 mmol) in chloroform (260 mL) was slowly added pyrrolidine (19 mL, 223.61 mmol) dropwise over a period of 1 hour at room temperature. The reaction mixture was continued to be stirred at room temperature for 1 hour before propargylamide (16 g, 223.61 mmol) was added. Subsequently, the reaction mixture was subjected to reflux in a Dean-Stark device for 16 hours. After completion of the reaction, the mixture was cooled and filtered. The filtrate was ground with toluene and filtered again. The filtrate was concentrated under reduced pressure to give a red to brown viscous liquid. The crude product was purified by fast column chromatography (silica gel, eluent 98:2 chloroform/methanol) to yield tert-butyl 2-oxo-1,2,7,8-tetrahydro-1,6-naphthyridine-6(5H)-carboxylate (4.01 g, 51.8% yield) as a brown oil.
References
[1] Patent: WO2009/121812, 2009, A1. Location in patent: Page/Page column 75-76
Tert-butyl 2-oxo-1,2,7,8-tetrahydro-1,6-naphthyridine-6(5h)-carboxylate Preparation Products And Raw materials
Raw materials
Preparation Products
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