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Chemical Structure| 1621225-24-8 Chemical Structure| 1621225-24-8

Structure of 1621225-24-8

Chemical Structure| 1621225-24-8

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Product Details of [ 1621225-24-8 ]

CAS No. :1621225-24-8
Formula : C12H17BClNO2
M.W : 253.53
SMILES Code : CC1(C(C)(OB(O1)C2=CC(Cl)=CN=C2C)C)C
MDL No. :MFCD18712496
InChI Key :BYJJEYBTKKFGST-UHFFFAOYSA-N
Pubchem ID :90319307

Safety of [ 1621225-24-8 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 1621225-24-8 ]

* 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 [ 1621225-24-8 ]

[ 1621225-24-8 ] Synthesis Path-Downstream   1~6

  • 1
  • [ 137628-17-2 ]
  • [ 1621225-24-8 ]
  • 2
  • [ 131036-39-0 ]
  • [ 73183-34-3 ]
  • [ 1621225-24-8 ]
YieldReaction ConditionsOperation in experiment
With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium acetate; In 1,4-dioxane; at 90℃; for 1.0h;Inert atmosphere; To a solution of 3-bromo-5-chloro-2-methylpyridine (0.60 g, 2.91 mmol) in 1,4-dioxane (12 mL) was added bis(pinacolato) diboron (1.47 g, 5.82 mmol), Pd(dppf)Cl2 (0.106 g, 0.145 mmol) and KOAc (0.857, 8.73 mmol). The mixture was sparged with Ar for 5 minutes and then the reaction was sealed and heated at 90 C for 1 hour. The reaction was then diluted with water (30 ml) and extracted with EtOAc (2 x 50 mL). The combined organic extracts were dried over anhydrous Na2S04, filtered, and concentrated under reduced pressure. The residue was purified on a silica gel column (0 to 50% EtOAc/hexanes) to afford 5-chloro-2-methyl-3-(4,4,5,5- tetramethyl-l,3,2-dioxaborolan-2-yl)pyridine. MS (ES) = 254 (M+l)+
With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium acetate; In 1,4-dioxane; at 25 - 80℃; for 2.0h;Inert atmosphere; To a solution of 3-bromo-5-chloro-2-methylpyridine (600 mg, 2.91 mmol, 1.00 eq) and Pin2B2 (886 mg, 3.49 mmol, 1 .20 eq) in dioxane (7.00 niL) were added Pd(dppf)Cl2 (213 mg, 291 umol, 0.100 eq) and KOAc (570 mg, 5.81 mmol, 2.00 eq) at 25C. The mixture was stirred at 80C for 2 h under N2. The mixture was concentrated under reduced pressure to give 5- chloro-2-methyl-3-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)pyridine (2.00 g, crude) as a black solid.
  • 3
  • [ 1621225-24-8 ]
  • tert-butyl (S)-4-bromo-12-fluoro-7a,13-dihydro-7H-[1,2,4]triazolo[4',3':1,6]pyrido[3,2-b]benzofuro[4,3-fg][1,4]oxazonine-14(8H)-carboxylate [ No CAS ]
  • tert-butyl (S)-4-(5-chloro-2-methylpyridin-3-yl)-12-fluoro-7a,13-dihydro-7H-[1,2,4]triazolo[4',3':1,6]pyrido[3,2-b]benzofuro[4,3-fg][1,4]oxazonine-14(8H)-carboxylate [ No CAS ]
YieldReaction ConditionsOperation in experiment
With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; sodium carbonate; In 1,4-dioxane; water; at 25 - 80℃; for 12.0h;Inert atmosphere; To a solution of tert-butyl (S)-4-bromo-12-fluoro-7a,13-dihydro-7H- [l,2,4]triazolo[4',3': l,6]pyrido[3,2-b]benzofuro[4,3-fg][l,4]oxazonine-14(8H)-carboxylate (100 mg, 204 umol, 1.00 e ) and 5-chJoro-2-methyJ-3-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2- yl)pyridine (310 mg, 1.22 mmol, 6.00 eq) in dioxane (4.00 mL) and water (0.800 niL) were added NaiCCb (43.2 mg, 407 umol, 2.00 eq) and Pd(dppf)Cl2 (14.9 mg, 20.4 umol, 0.100 eq) at 25C. The mixture was stirred at 80C for 12 h under N?.. The mixture was combined with the other batches (from 100 mg of tert-butyl (S)-4-bromo-12-fluoro-7a, 13-dihydro-7H- [ 1 ,2,4]triazoio[4',3 : 1 ,6]pyrido[3 ,2-b]benzofuro[4,3 -fg] [ 1 ,4]oxazonine- 14(8H)-carboxylate). The mixture was filtered and the filtrate was concentrated under reduced pressure. The residue was purified by prep- TLC (S1O2, Petroleum etherEthyl acetate = 1 : 1) to give tert-butyl (S)-4-(5- chloro-2-methylpyridin-3-yl)-12-fluoro-7a, 13-dihydro-7H-[l,2,4]triazolo[4',3': l,6]pyrido[3,2- b]benzofuro[4,3-fg][l,4]oxazonine-14(8H)-carboxylate (150 mg, crude) was obtained as yellow oil.
  • 4
  • [ 1621225-24-8 ]
  • tert-butyl (S)-4-bromo-12-fluoro-7a,13-dihydro-7H-[1,2,4]triazolo[4',3':1,6]pyrido[3,2-b]benzofuro[4,3-fg][1,4]oxazonine-14(8H)-carboxylate [ No CAS ]
  • (S)-4-(5-chloro-2-methylpyridin-3-yl)-12-fluoro-7a,13-dihydro-7H-[1,2,4]triazolo[4',3':1,6]pyrido[3,2-b]benzofuro[4,3-fg][1,4]oxazonine hydrochloride [ No CAS ]
  • 5
  • [ 186593-43-1 ]
  • [ 1621225-24-8 ]
  • 6
  • [ 186593-42-0 ]
  • [ 1621225-24-8 ]
 

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