tert-butyl 2-chloro-7,8-dihydro-1,6-naphthyridine-6(5H)-carboxylate
tert-butyl 2-chloro-7,8-dihydro-1,6-naphthyridine-6(5H)-carboxylate Basic information
- Product Name:
- tert-butyl 2-chloro-7,8-dihydro-1,6-naphthyridine-6(5H)-carboxylate
- Synonyms:
-
- tert-butyl 2-chloro-7,8-dihydro-1,6-naphthyridine-6(5H)-carboxylate
- tert-butyl 2-chloro-7,8-dihydro-1,6-naphthyridine-6(5H)-carboxyl
- tert-butyl 2-chloro-5,6,7,8-tetrahydro-1,6-naphthyridine-6-carboxylate
- 2-chloro-7,8-dihydro-, 1,1-diMethylethyl ester
- 1,6-Naphthyridine-6(5H)-carboxylic acid, 2-chloro-7,8-dihydro-, 1,1-dimethylethyl ester
- ert-butyl 2-chloro-7,8-dihydro-1,6-naphthyridine-6(5H)-carboxylate
- tert-Butyl 2-chloro-7,8-dihydro-1,6-naphthyridine-6(5H)
- tert-butyl 2-chloro-7,8-dihydro-5H-1,6-naphthyridine-6-carboxylate
- CAS:
- 1151665-15-4
- MF:
- C13H17ClN2O2
- MW:
- 268.74
- Product Categories:
-
- Heterocycle-Pyridine series
- Mol File:
- 1151665-15-4.mol
tert-butyl 2-chloro-7,8-dihydro-1,6-naphthyridine-6(5H)-carboxylate Chemical Properties
- Boiling point:
- 372.9±42.0 °C(Predicted)
- Density
- 1.223
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- pka
- 0.58±0.20(Predicted)
- Appearance
- White to off-white Solid
tert-butyl 2-chloro-7,8-dihydro-1,6-naphthyridine-6(5H)-carboxylate Usage And Synthesis
Synthesis
766545-20-4
24424-99-5
1151665-15-4
A slurry was formed in dichloromethane (DCM, 1 L) using 2-chloro-5,6,7,8-tetrahydro-1,6-naphthyridine hydrochloride (106.1 g, 517 mmol) and N,N-diisopropylethylamine (80 g, 108 mL, 621 mmol, 1.2 equiv.) as starting materials. A solution of di-tert-butyl dicarbonate (119 g, 543 mmol, 1.05 eq.) in DCM (100 mL) was slowly added through the addition funnel over a period of 1 hour. The reaction mixture was gradually converted to a clarified solution, followed by continued stirring at room temperature for 1 h. The reaction progress was monitored by LCMS. Upon completion of the reaction, the mixture was concentrated. The concentrated residue was dissolved in ethyl acetate (EtOAc, 1 L), washed sequentially with water (3 x 300 mL) and brine (300 mL), and the organic phase was dried with anhydrous magnesium sulfate (MgSO4). The solvent was removed by evaporation under reduced pressure to afford 2-chloro-7,8-dihydro-1,6-naphthyridine-6(5H)-carboxylic acid 1,1-dimethylethyl ester as an off-white solid (139 g, yield: 100%). The product was characterized by 1H NMR (400 MHz, CDCl3) and LCMS: 1H NMR δ 1.49 (9H, s), 2.97 (2H, t, J = 5.9 Hz), 3.73 (2H, t, J = 6.0 Hz), 4.57 (2H, s), 7.17 (1H, d, J = 8.0 Hz), 7.38 (1H, d, J = 8.0 Hz) ppm; LCMS m/z: 269 (M + 1).
References
[1] Patent: US2012/244110, 2012, A1. Location in patent: Page/Page column 61
[2] Journal of Medicinal Chemistry, 2014, vol. 57, # 8, p. 3430 - 3449
[3] Patent: EP3252059, 2017, A1. Location in patent: Paragraph 0335; 0338; 0339
[4] Patent: WO2009/121812, 2009, A1. Location in patent: Page/Page column 78
[5] Patent: WO2013/79452, 2013, A1. Location in patent: Page/Page column 138; 139
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