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Chemical Structure| 58885-35-1 Chemical Structure| 58885-35-1

Structure of 58885-35-1

Chemical Structure| 58885-35-1

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Product Details of [ 58885-35-1 ]

CAS No. :58885-35-1
Formula : C23H23NO2S
M.W : 377.50
SMILES Code : N[C@@H](CSC(C1=CC=CC=C1)(C2=CC=CC=C2)C3=CC=CC=C3)C(OC)=O

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Application In Synthesis of [ 58885-35-1 ]

* 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 [ 58885-35-1 ]

[ 58885-35-1 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 2799-07-7 ]
  • [ 77-76-9 ]
  • [ 58885-35-1 ]
  • 2
  • [ 58885-35-1 ]
  • [ 166737-85-5 ]
YieldReaction ConditionsOperation in experiment
57% With ammonia; In methanol; at -78 - 20℃; for 14h; To 2.68g (7.37 mmol) of S-trityl-L-cysteine and 40 mL of methanol was added 7 mL (96 mmol) of thionyl chloride dropwise. After heating at reflux for 6h the solution was cooled to room temperature and then concentrated in vacuo. The resulting residue was taken up in 20 mL of methanol, treated with activated carbon, filtered and concentrated in vacuo yielding the methyl ester as an off-white foam. This material was dissolved in 6 mL of methanol in a sealable tube and cooled to -78. After 30 mL of liquid ammonia was added, the tube was sealed and the reaction was stirred at room temperature for 14h After recooling to -78 the reaction tube was unsealed and the solution was carefully reduced to dryness. The residue was chromatographed on silica gel eluting with methylene chloride/methanol (10:1) furnishing 1.52g (57%) of the primary amide as a white solid. Electrospray Mass Spec: 363.2 (M+H)+
  • 3
  • [ 2799-07-7 ]
  • [ 58885-35-1 ]
YieldReaction ConditionsOperation in experiment
With methanol;Heating / reflux; To 2.68g (7.37 mmol) of <strong>[2799-07-7]S-trityl-L-cysteine</strong> and 40 mL of methanol was added 7 mL (96 mmol) of thionyl chloride dropwise. After heating at reflux for 6h the solution was cooled to room temperature and then concentrated in vacuo. The resulting residue was taken up in 20 mL of methanol, treated with activated carbon, filtered and concentrated in vacuo yielding the methyl ester as an off-white foam. This material was dissolved in 6 mL of methanol in a sealable tube and cooled to -78°. After 30 mL of liquid ammonia was added, the tube was sealed and the reaction was stirred at room temperature for 14h After recooling to -78° the reaction tube was unsealed and the solution was carefully reduced to dryness. The residue was chromatographed on silica gel eluting with methylene chloride/methanol (10:1) furnishing 1.52g (57percent) of the primary amide as a white solid. Electrospray Mass Spec: 363.2 (M+H)+
  • 4
  • [ 67-56-1 ]
  • [ 2799-07-7 ]
  • [ 58885-35-1 ]
YieldReaction ConditionsOperation in experiment
81% With sulfuric acid; for 4h;Reflux; Compound 3 (500 mg, 1.38 mmol) was dissolved in well-dried methanol (8 mL) and was stirred under reflux catalyzed by concentrated sulfuric acid (0.5 mL). After 4 h, the solvent was removed under reduced pressure and the crude product was extracted with ethyl acetate and washed with saturated sodium bicarbonate for several times. The organic layer was dried over anhydrous magnesium sulfate, filtered and concentrated to give ester 4 (420 mg, 81percent) as a yellow viscous oil. 1H NMR (300 MHz, CDCl3): delta = 7.45-7.18 (m, 15H), 3.66 (s, 3H), 3.20 (q, J = 7.61 Hz, 4.94 Hz, 1H), 2.59 (dd, J = 12.5 Hz, 4.76 Hz, 1H), 2.47 (dd, J = 12.4 Hz, 7.76 Hz, 1H), 1.65 (s, 2H). 13C NMR (75 MHz, CDCl3): delta = 173.61, 144.15, 129.11, 127.53, 126.34, 66.31, 53.28, 51.58, 36.46. MALDI-TOF-MS: Calcd for C23H23KNO2S 416.1. Found 416.1 [M+K]+.
75% With sulfuric acid; for 12h;Reflux; A solution of 2[36] and [37] (590, 1.5 mmol) and H2SO4 concentrated (200 muL) in MeOH (5 mL) was refluxed for 12 h. The solvent was then evaporated in vacuo and the residue obtained was dissolved in H2O and extracted with AcOEt. The organic phase was dried, filtered and evaporated to give a crude residue purified by chromatography over silica gel (Eluent: CH2Cl2/MeOH = 93:7) to afford product 5 (420 mg, 75percent) as white foam.1H NMR (DMSO): delta (ppm) 2.20-2.41 (m, 2H, CH2); 3.15-3.20 (m, 1H, CH); 3.57 (s, 3H, OCH3); 7.24-7.35 (m, 15H, trityl-H).MALDI-TOF MS: m/z 378.7 Da [M + H]+, C23H23NO2S, Mol. Wt.: 377.50.
72% With thionyl chloride; at 80℃;Cooling with ice; Synthetic Example 30; (R)-Methyl 3-mercapto-2-(5-morphoIinopentanamido)propanoate; Step 1 : (RVmethyl 2-(5-bromopentanamido)-3-(tritylsulfanyDpropanoate; Thionyl chloride (8.2 g, 68.9 mmol) was added to MeOH (500 mL) slowly with ice-cooling, and then S-trityl cysteine (25.0 g, 68.9 mmol) was added to the solution. The resulting mixture was continuously stirred overnight at 80°C. The solvent was concentrated by reduced pressure and purified by column chromatography with DCM:MeOH = 10:1 to afford S-trityl cysteine methyl ester as a white solid. (18.6 g, 72percent yield).
 

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