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Chemical Structure| 944902-70-9 Chemical Structure| 944902-70-9

Structure of 944902-70-9

Chemical Structure| 944902-70-9

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Product Details of [ 944902-70-9 ]

CAS No. :944902-70-9
Formula : C8H11N3O
M.W : 165.19
SMILES Code : COC1=C(CNCC2)C2=NC=N1
MDL No. :MFCD10697114

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Application In Synthesis of [ 944902-70-9 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 944902-70-9 ]

[ 944902-70-9 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 944902-70-9 ]
  • [ 848366-28-9 ]
  • [ 1354691-64-7 ]
YieldReaction ConditionsOperation in experiment
19% With sodium t-butanolate;palladium diacetate; XPhos; In toluene; tert-butyl alcohol; at 20 - 110℃; for 122.0h;Inert atmosphere; Intermediate 15: 6-(5-Chloro-6-methoxy-pyridin-3-yl)-4-methoxy-5,6,7,8-tetrahydro- pyrido[4,3-d]pyrimidine; To a glass vial was added 4-methoxy-5,6,7,8-tetrahydro-pyrido[4,3-d]pyrimidine (WO2008/130481 , p 47) (0.273 g, 1 .65 mmol), <strong>[848366-28-9]5-bromo-3-chloro-2-methoxypyridine</strong> (0.368 g, 1.65 mmol), sodium ferf-butoxide (318 mg, 3.31 mmol), diacetoxypalladium (0.037 g, 0.17 mmol), X-Phos (0.079 g, 0.17 mmol) and anhydrous toluene / ferf-butanol, 5 /1 (6 mL). The vial was flushed with a stream of argon for 15 sec and capped. The mixture was heated with stirring for 2h at 1 10C then allowed to cool to room temperature and stirred at rt for 5 days. Diluted with CH2CI2 (10 mL) and water (2 mL), filtered through a celite pad. The organic phase was separated by filtering through a phase separation tube and concentrated in vacuo. Purified by flash chromatography on silica gel with heptane / EtOAc 100 / 0 to 0/ 100 to give 6-(5-chloro-6-methoxy-pyridin-3-yl)-4-methoxy-5,6,7,8-tetrahydro-pyrido[4,3- d]pyrimidine as a yellow solid (95 mg, 19% yield) LCMS: [M+H]+=307.0 / 308.9, Rt (3)= 1 .62 mm.
19% With palladium diacetate; sodium t-butanolate; XPhos; In toluene; tert-butyl alcohol; at 20 - 110℃; for 122.0h;Inert atmosphere; To a glass vial was added 4-methoxy-5,6,7,8-tetrahydro-pyrido[4,3-d]pyrimidine (WO 2008/130481 , p 47) (0.273 g, 1.65 mmol), <strong>[848366-28-9]5-bromo-3-chloro-2-methoxypyridine</strong> (0.368 g, 1.65 mmol), sodium ferf-butoxide (318 mg, 3.31 mmol), diacetoxypalladium (0.037 g, 0.17 mmol), X-Phos (0.079 g, 0.17 mmol) and anhydrous toluene / ferf-butanol, 5 /1 (6 mL). The vial was flushed with a stream of argon for 15 sec and capped. The mixture was heated with stirring for 2h at 1 10C then allowed to cool to room temperature and stirred at rt for 5 days. Diluted with CH2CI2 (10 mL) and water (2 mL), filtered through a celite pad. The organic phase was separated by filtering through a phase separation tube and concentrated in vacuo. Purified by flash chromatography on silica gel with heptane / EtOAc 100 / 0 to 0/ 100 to give 6-(5-chloro-6-methoxy-pyridin-3-yl)-4-methoxy-5,6,7,8-tetrahydro-pyrido[4,3-d]pyrimidine as a yellow solid (95 mg, 19% yield) LCMS: [M+H]+=307.0 / 308.9, Rt (3)= 1.62 mm.
19% With palladium diacetate; sodium t-butanolate; XPhos; In toluene; tert-butyl alcohol; at 20 - 110℃; for 122.0h;Inert atmosphere; Intermediate 15 6-(5-Chloro-6-methoxy-pyridin-3-yl)-4-methoxy-5,6,7,8-tetrahydro-pyrido[4,3-d]pyrimidine To a glass vial was added 4-methoxy-5,6,7,8-tetrahydro-pyrido[4,3-d]pyrimidine (WO 2008/130481, p 47) (0.273 g, 1.65 mmol), <strong>[848366-28-9]5-bromo-3-chloro-2-methoxypyridine</strong> (0.368 g, 1.65 mmol), sodium tert-butoxide (318 mg, 3.31 mmol), diacetoxypalladium (0.037 g, 0.17 mmol), X-Phos (0.079 g, 0.17 mmol) and anhydrous toluene/tert-butanol, 5/1 (6 mL). The vial was flushed with a stream of argon for 15 sec and capped. The mixture was heated with stirring for 2 h at 110 C. then allowed to cool to room temperature and stirred at rt for 5 days. Diluted with CH2Cl2 (10 mL) and water (2 mL), filtered through a celite pad. The organic phase was separated by filtering through a phase separation tube and concentrated in vacuo. Purified by flash chromatography on silica gel with heptane/EtOAc 100/0 to 0/100 to give 6-(5-chloro-6-methoxy-pyridin-3-yl)-4-methoxy-5,6,7,8-tetrahydro-pyrido[4,3-d]pyrimidine as a yellow solid (95 mg, 19% yield) LCMS: [M+H]+=307.0/308.9, Rt(3)=1.62 min.
  • 2
  • [ 109229-22-3 ]
  • [ 944902-70-9 ]
 

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