Home Cart Sign in  
Chemical Structure| 60971-72-4 Chemical Structure| 60971-72-4

Structure of 60971-72-4

Chemical Structure| 60971-72-4

*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 [ 60971-72-4 ]

CAS No. :60971-72-4
Formula : C5H4ClNOS
M.W : 161.61
SMILES Code : O=C(Cl)C1=CN=C(C)S1
MDL No. :MFCD13173719

Safety of [ 60971-72-4 ]

Application In Synthesis of [ 60971-72-4 ]

* 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 [ 60971-72-4 ]

[ 60971-72-4 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 280-57-9 ]
  • [ 40004-69-1 ]
  • [ 60971-72-4 ]
YieldReaction ConditionsOperation in experiment
96.0% and 92.8% In 5,5-dimethyl-1,3-cyclohexadiene; EXAMPLE 14 In a similar apparatus to Example 1, 10.0 g (0.07 mole) of <strong>[40004-69-1]2-methylthiazole-5-carboxylic acid</strong> were suspended in 100 ml of xylene, followed by the addition of 0.03 g of triethylenediamine. Under heating and reflux, phosgene was blown at a rate of 930 ml/hr for 6 hours (0.25 mole). After completion of the blowing, stirring was continued for additional 2 hours. After completion of the reaction, the reaction mixture was filtered and the filtrate was concentrated to obtain 10.5 g of <strong>[40004-69-1]2-methylthiazole-5-carboxylic acid</strong> chloride. Its purity and yield were 96.0percent and 92.8percent, respectively.
  • 2
  • [ 40004-69-1 ]
  • [ 60971-72-4 ]
YieldReaction ConditionsOperation in experiment
95.0% and 95.0% In toluene; EXAMPLE 5 In a similar apparatus to Example 1,5.7 g (0.04 mole) of <strong>[40004-69-1]2-methylthiazole-5-carboxylic acid</strong> were suspended in 100 ml of toluene. Under heating and reflux, phosgene was blown at a rate of 390 ml/hr for 10 hours (0.17 mole). After completion of the blowing, stirring was continued for additional 2 hours. After completion of the reaction, the reaction mixture was filtered and the filtrate was concentrated to obtain 5.7 g of <strong>[40004-69-1]2-methylthiazole-5-carboxylic acid</strong> chloride. Its purity and yield were 95.0percent and 95.0percent, respectively. NMR (deltaCDCl 3/TMS, ppm): 2.79(3H,s).
With oxalyl dichloride;N,N-dimethyl-formamide; In dichloromethane; at 20℃; for 0.5h;Product distribution / selectivity; Ethyl 2-methyl-1,3-thiazole-5-carboxylate [e.g. available from Interchim S.A.] (61 mg) in ethanol (1 ml) was treated with aqueous sodium hydroxide (2M, 0.706 ml). The clear solution was stirred at room temperature for 18 h and then treated with aqueous hydrochloric acid (2M, 0.54 ml). The solution was blown down to dryness and the residual solid dried under vacuum over phosphorus pentoxide. The solid was then suspended in dry dichloromethane (1 ml) and treated at 20° C. with oxalyl chloride (0.032 ml) and DMF (1 drop). The mixture was stirred at room temperature for 30 mins and was then added dropwise to a solution of Intermediate 16 (98 mg) in anhydrous acetonitrile (2 ml). DIPEA (0.064 ml) was added and the solution stirred at room temperature for 20 h. The mixture was diluted with dichloromethane (15 ml), washed with dilute aqueous sodium chloride (2.x.15 ml) and blown down to dryness. The residue was purified by mass directed autoprep HPLC to give a film which was further purified using an SPE cartridge (2 g, aminopropyl) which had been pre-washed with methanol. Elution with methanol gave Example 311 as a white solid (87 mg). LCMS showed MH+=429; TRET=1.94 min.
With oxalyl dichloride;N-formyldiethylamine; In dichloromethane; for 0.25h;Product distribution / selectivity; 2-Methyl-1,3-thiazole-5-carboxylic acid (0.133 g, 0.93 mmol) (e.g. which can optionally be prepared as in Example 311) was suspended in dichloromethane (3 ml) and treated at 20° C. under nitrogen with oxalyl chloride (0.24 ml, 2.75 mmol) and diethylformamide (1 drop). A vigorous reaction occurred. After 15 min, the reaction mixture was evaporated to dryness to give a dark yellow oil which was presumed to be 2-methyl-1,3-thiazole-5-carbonyl chloride.
With oxalyl dichloride;N,N-dimethyl-formamide; In dichloromethane; at 20℃; for 0.5h; Example 311 N-[1,6-diethyI-4-(tetrahydro-2H-pyran-4-yIamino)-1H- pyrazoIo[3,4-b]pyridin-5-yl]methyl}-2-methyI-1,3-thiazole-5-carboxamideEthyl 2-methyl-1 ,3-thiazole-5-carboxylate [e.g. available from lnterchim S.A.] (61 mg) in ethanol (1ml) was treated with aqueous sodium hydroxide (2M, 0.706ml). The clear solution was stirred at room temperature for 18h and then treated with aqueous hydrochloric acid (2M, 0.54ml). The solution was blown down to dryness and the residual solid dried under vacuum over phosphorus pentoxide. The solid was then suspended in dry dichloromethane (1ml) and treated at 20°C with oxalyl chloride (0.032ml) and DMF (1 drop). The mixture was stirred at room temperature for 30mins and was then added dropwise to a solution of Intermediate 16 (98mg) in anhydrous acetonitrile (2ml). DIPEA (0.064ml) was added and the solution stirred at room temperature for 2Oh. The mixture was diluted with dichloromethane (15ml), washed with dilute aqueous sodium chloride (2 x 15ml) and blown down to dryness. The residue was purified by mass directed autoprep HPLC to give a film which was further purified using an SPE cartridge (2g, aminopropyl) which had been pre-washed with methanol. Elution with methanol gave Example 311 as a white solid (87mg). LCMS showed MH+ =

  • 3
  • [ 79836-78-5 ]
  • [ 60971-72-4 ]
 

Historical Records