Home Cart Sign in  
Chemical Structure| 454483-81-9 Chemical Structure| 454483-81-9

Structure of 454483-81-9

Chemical Structure| 454483-81-9

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

4.5 *For Research Use Only !

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

US Stock

Global Stock

In Stock
{[ item.pr_size ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

  • {[ item.pr_size ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of [ 454483-81-9 ]

CAS No. :454483-81-9
Formula : C5H3BrN2S
M.W : 203.06
SMILES Code : N#CC1=CSC(CBr)=N1
MDL No. :MFCD24459268

Safety of [ 454483-81-9 ]

Application In Synthesis of [ 454483-81-9 ]

* 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 [ 454483-81-9 ]

[ 454483-81-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 21917-76-0 ]
  • [ 454483-81-9 ]
YieldReaction ConditionsOperation in experiment
83% With N-Bromosuccinimide; dibenzoyl peroxide; In tetrachloromethane; at 95℃; for 15h; To a mixture of 2-METHYL-THIAZOLE-4-CARBONITRILE (3.0 g, 24.1 mmol), N bromosuccinimide (4.3 g, 24.1 mmol) in CC14 (50 mL) was added benzoyl peroxide (0.583 g, 0.10 mmol). The resulting mixture was stirred at 95C for 15 h, concentrated under reduced pressure, diluted with EtOAc (100 mL) and washed with saturated NA2S203 (50 ML), NAHC03 (50 ML) and brine (20 mL). The organic phase was dried over sodium sulfate and concentrated under reduced pressure. The crude residue was purified via silica gel column chromatography using EtOAc/n-hexane as eluent to afford the title compound (4.6 g, 83%) as yellow oil. RF 0. 39 (silica gel, EtOAc/hexane, 3/7).
47% With N-Bromosuccinimide; dibenzoyl peroxide; In benzene; Example 393A 2-(bromomethyl)-1,3-thiazole-4-carbonitrile To a solution of 2-methyl-1-thiazole-4-carbonitrile (248 mg, 2 mmol) in benzene (20 mL) was added N-bromosuccinimide (1.78 g, 10 mmol) and dibenzoyl peroxide (20 mg, 0.08 mmol). The mixture was refluxed for 2 days. The solution was evaporated under reduced pressure. The residue was partitioned between dichloromethane and water. The organic layer was concentrated under reduced pressure and the residue was chromatographed on silica gel eluding with 1:1 dichloromethane:hexane to give the title compound (190 mg, 47%).
With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); In tetrachloromethane; 2-Bromomethyl-thiazole-4-carbonitrile was prepared from 2-methyl-1, 3-thiazole-4- carbonitrile (124 mg, 1.0 mmol) with NBS (199.3 mg, 1.12 mmol) and AIBN (18.4 mg) in [TETRACHLOROCARBON (2 ML).] 2- {2-[3-(3-Cyano-phenyl)-[1, 2,4] [OXADIAZOL-5-YL]-PIPERIDIN-1-] [YLMETLZYL}-THIAZOLE-4-CARBONITRILE] (56 mg, 74.4%) was obtained from [3- (5-PIPERIDIN-2-YL-] [[1,] 2,4] oxadiazol-3-yl) -benzonitrile (50.8mg, 0.2 mmol) with crude 2-bromomethyl- [THIAZOLE-4-CARBONITRILE] (1.0 mmol) and diisopropylethylamine (129.25 mg, 1.0 mmol) in DMF (1.5 mL) at 80 C for 20 h. 1H NMR [(CDC13),] 8 (ppm): 8.38 (d, 1H), 8.31 (dd, [1H),] 7.97 (s, [1H),] 7. [80] (dd, [1H),] 7.62 (d, [1H),] 4. [30] (t, [1H),] 4.00 (dd, 2H), 3.07 (m, [1H),] 2.62 (m, 1H), 2.11 (m, 2H), 1.60-1. 80 (m, 4H).
 

Historical Records