Home Cart 0 Sign in  

[ CAS No. 1000160-74-6 ] {[proInfo.proName]}

,{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]}
Chemical Structure| 1000160-74-6
Chemical Structure| 1000160-74-6
Structure of 1000160-74-6 * Storage: {[proInfo.prStorage]}
Cart0 Add to My Favorites Add to My Favorites Bulk Inquiry Inquiry Add To Cart

Quality Control of [ 1000160-74-6 ]

Related Doc. of [ 1000160-74-6 ]

Alternatived Products of [ 1000160-74-6 ]

Product Details of [ 1000160-74-6 ]

CAS No. :1000160-74-6 MDL No. :MFCD16995819
Formula : C14H17BO2S Boiling Point : -
Linear Structure Formula :- InChI Key :PNPHOIZEFCAWEB-UHFFFAOYSA-N
M.W : 260.16 Pubchem ID :66673976
Synonyms :

Safety of [ 1000160-74-6 ]

Signal Word:Warning Class:
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330 UN#:
Hazard Statements:H302-H315-H319 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 1000160-74-6 ]

* 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 [ 1000160-74-6 ]

[ 1000160-74-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1000160-74-6 ]
  • [ 153034-94-7 ]
  • [ 1034658-77-9 ]
YieldReaction ConditionsOperation in experiment
82% With sodium carbonate;dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; johnphos; In tetrahydrofuran; water; at 100℃; for 3h; Preparation 18; 4-Benzo[£]thiophen-7-yl-2-fluoro-5-methyl-pyridine; In a flask, combine <strong>[153034-94-7]2-fluoro-4-iodo-5-methyl-pyridine</strong> (355 mg, 1.5 mmol), 2- benzo[£]thiophen-7-yl-4,4,5,5-tetramethyl-[l,3,2]dioxaborolane (282 mg, 1.8 mmol), [l,r-bis(diphenylphosphino)ferrocene]dichloropalladium(II), complex with dichloromethane (1: 1) (61 mg, 0.07 mmol), 2-(di-tert-butylphosphino)biphenyl (13 mg, 0.04 mmol), sodium carbonate (2 M, 1.5 mL, 3 mmol) and THF (10 mL). Heat the mixture at 100 0C for 3 hours in an oil bath. Dilute the mixture with chloroform/isopropanol (3/1). Wash the solution with saturated aqueous sodium chloride. Dry over sodium sulfate. Concentrate in vacuo to a dark residue. Purify by column chromatography (20 % ethyl acetate in hexane) to afford the title compound (300 mg, 82 %) as yellow oil. MS (ES) m/z 244 [M+ 1]+.
82% With sodium carbonate; johnphos;(1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In tetrahydrofuran; at 100℃; for 3h; Preparation 844-Benzo[b]thiophen-7-yl-2-fluoro-5-methyl-pyridineIn a flask, combine <strong>[153034-94-7]2-fluoro-4-iodo-5-methyl-pyridine</strong> (355 mg,1.5 mmol), 2- benzo[b]thiophen-7-yl-4,4,5,5-tetramethyl-[l,3,2]dioxaborolane (282 mg, 1.8 mmol), Pd(dppf)Cl2 (61 mg, 0.07 mmol), 2-(di-tert-butylphos-phino)biphenyl (13 mg, 0.04 mmol), sodium carbonate (2 M, 1.5 mL, 3 mmol) and THF (10 mL). Heat the mixture at 100 0C for 3 h in an oil bath. Dilute the mixture with chloroform/IPA (3/1). Wash the solution with aqueous saturated sodium chloride. Dry over sodium sulfate. Concentrate in vacuo to a dark residue. Purify by column chromatography (20 % ethyl acetate in hexane) to afford the title compound (300 mg, 82 %) as a yellow oil. MS (ES) m/z 244
Same Skeleton Products
Historical Records