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Chemical Structure| 138232-44-7 Chemical Structure| 138232-44-7

Structure of 138232-44-7

Chemical Structure| 138232-44-7

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Product Details of [ 138232-44-7 ]

CAS No. :138232-44-7
Formula : C13H17NO5S
M.W : 299.34
SMILES Code : O=C(N1CC(OS(=O)(C)=O)CC1)OCC2=CC=CC=C2
MDL No. :MFCD16620796

Safety of [ 138232-44-7 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis of [ 138232-44-7 ]

* 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 [ 138232-44-7 ]

[ 138232-44-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 124-63-0 ]
  • [ 95656-88-5 ]
  • [ 138232-44-7 ]
YieldReaction ConditionsOperation in experiment
80% With triethylamine; In dichloromethane; Compound 26 (2.6 g, 11.8 mmol) and triethylamine (3.3 mL,17.6 mmol) were added in dichloromethane (30 ml). Methanesulfonylchloride (1.4 mL, 17.6 mmol) was added dropwise andthe mixture was kept below 5 C and then heated to 25 C for 3.5 h.The reaction was monitored by TLC. After the end of the reaction,the mixture was filtered and the filtrate was washed with 1M HCl(20 mL), saturated aqueous solution of sodium bicarbonate (20 mL)and brine (20 mL). Then the mixture was dried by anhydrous sodiumsulfate and filtered. The filtrate was evaporated underreduced pressure to give an oily compound (3.1 g, 80% yield). 1HNMR (300 MHz, DMSO-d6): delta= 7.35 (m, 5H, Ar-H), 5.22 (s, 2H,OCH2-Ar), 5.09 (m, 1H, OCH(CH2)2), 3.78 (m, 2H, CHCH2N), 3.56 (m,2H, CHCH2CH2N), 3.09 (s, 3H, SO2CH3), 2.05 (m, 2H, CHCH2CH2N)ppm.
In pyridine; (R)-3-(Methylsulfonyl)oxy]-1-pyrrolidinecarboxylic acid, phenylmethyl ester A solution of 17.5 g (84 mmol) of (R)-3-hydroxy-1-pyrrolidinecarboxylic acid, phenylmethyl ester in 150 ml of dry pyridine was cooled to 5 and treated dropwise with 11.5 g (0.1 mol) of methanesulfonyl chloride keeping the temperature at 5. The reaction mixture was stirred at 5 for two hours and stored at 5 for 18 hours. The reaction mixture was allowed to warm to room temperature over three hours and the solvent was then removed in vacuo. The residue was partitioned between ethyl acetate/water (500 ml each) and the aqueous layer was reextracted with ethyl acetate. The combined organic layers were washed with water, dried (MgSO4), and evaporated in vacuo to give 21.2 g of the title compound.
In pyridine; (R)-3-[(Methylsulfonyl)oxy]-1-pyrrolidinecarboxylic acid, phenylmethyl ester A solution of 17.5 g (84 mmol) of (R)-3-hydroxy-1-pyrrolidinecarboxylic acid, phenylmethyl ester in 150 ml of dry pyridine was cooled to 5 and treated dropwise with 11.5 g (0.1 mol) of methanesulfonyl chloride keeping the temperature at 5. The reaction mixture was stirred at 5 for two hours and stored at 5 for 18 hours. The reaction mixture was allowed to warm to room temperature over three hours and the solvent was then removed in vacuo. The residue was partitioned between ethyl acetate/water (500 ml each) and the aqueous layer was reextracted with ethyl acetate. The combined organic layers were washed with water, dried (MgSO4) and evaporated in vacuo to give 21.2 g of the title compound.
With triethylamine; In dichloromethane; at 0 - 20℃; for 2h;Inert atmosphere; Step 1 Benzyl 3-((methylsulfonyl)oxy)pyrrolidine-1 -carboxylateTo a stirred solution of <strong>[95656-88-5]benzyl 3-hydroxypyrrolidine-1-carboxylate</strong> (500 mg, 2.26 mmol) in DCM (10 mL) was added triethylamine (686 mg, 0,94 mL, 6.78 mmol) at room temperature. The resulting mixture was cooled to 0 C. Then methanesulfonyl chloride (388 mg, 3.39 mmol) was added dropwise into the mixture and the mixture was slowly warmed to room temperature over 2his under N2 atomsphere. The mixture was diluted with DCM (20 mL) and washed with H20 (10 mE x 2), hydrochloric acid (10 ml x 2, iN), saturated NaHCO3 (10 mE). The organic phase was dried over anhydrous Na2SO4, filtered and concentrated to give the crude desired product (600 mg) as a brown oil which was used in the next step without further purification.
With triethylamine; In dichloromethane; at 20℃; for 3h;Cooling with ice; TDI01272-2 (5.20 g, 23.6 mmol) was dissolved in dichloromethane (150 mL), triethylamine (7.15 g, 70.8 mmol)was added, and methylsulfonyl chloride (4.04 g, 35.5 mmol) was added under ice bath cooling. The reaction wasperformed at room temperature for 3 h. Thin layer chromatography indicated the reaction was complete. The reactionsolution was quenched by water (100 mL), and extracted with dichloromethane (300 mL). The combined organic phasewas washed with saturated brine (400 mL), dried over anhydrous sodium sulfate, filtered, and concentrated underreduced pressure to afford TDI01272-3 (7.50 g, yellow oil, crude product).1H NMR (400 MHz, CDCl3) delta 7.33 - 7.29 (m, 4H), 7.28 - 7.24 (m, 1H), 5.21 - 5.15 (m, 1H), 3.68 (d, J = 12.8 Hz, 1H),3.62 (d, J = 12.8 Hz, 1H), 2.98 (s, 3H), 2.86 - 2.78 (m, 3H), 2.53 - 2.47 (m, 1H), 2.35 - 2.28 (m, 1H), 2.11 - 2.04 (m, 1H).

 

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