Pharmaceutical

59279-60-6

  • Product Name:(R)-N-Boc-glutamic acid-1,5-dimethyl ester
  • Molecular Formula:C12H21NO6
  • Specifications:99%
  • Molecular Weight:275.302
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Product Details;

CasNo: 59279-60-6

Molecular Formula: C12H21NO6

Factory supply (R)-N-Boc-glutamic acid-1,5-dimethyl ester 59279-60-6 with sufficient stock and high standard

  • Molecular Formula:C12H21NO6
  • Molecular Weight:275.302
  • Vapor Pressure:1.07E-05mmHg at 25°C 
  • Melting Point:43.0 to 47.0 °C 
  • Refractive Index:1.452 
  • Boiling Point:370.9 °C at 760 mmHg 
  • PKA:10.86±0.46(Predicted) 
  • Flash Point:178.1 °C 
  • PSA:90.93000 
  • Density:1.117g/cm3 
  • LogP:1.39680 

(R)-N-Boc-glutamic acid-1,5-dimethyl ester(Cas 59279-60-6) Usage

Synthesis

L-glutamic acid (10.0 g, 67.97 mmol) was dissolved in 200 mL of methanol, and SOCl2(10.85 mL, 149.53 mmol)was slowly added dropwise under an ice bath. After the addition, reflux was performed at 65 ° C. After 2 hours, the reaction system was cooled to room temperature, and methanol was evaporated to dryness under reduced pressure to obtain a colorless viscous substance.This colorless viscous substance was dissolved in 200 mL of THF, (Boc)2O (22.25 g, 101.95 mmol) was addedunder an ice bath, and triethylamine (14.13 mL, 101.95 mmol) was slowly added dropwise.After the addition was complete, the reaction was allowed to proceed at room temperature overnight.After completion of the reaction, the solvent was distilled off under reduced pressure.The residue was dissolved in 200 mL of dichloromethane.The organic phase was washed with water (200 mL * 2), saturated citric acid solution (200 mL * 2), saturated sodium bicarbonate solution (200 mL * 2), and saturated brine (200 mL * 2) in that order.The organic phase was dried over anhydrous Na2SO4. Thefiltrate was collected by filtration, and the solvent was evaporated under reduced pressure. The residue was purified by column chromatography (petroleum ether: ethyl acetate = 4: 1 v / v) to give a colorless oily product 2 (18.34 g, yield 98%)

InChI:InChI=1/C12H21NO6/c1-12(2,3)19-11(16)13-8(10(15)18-5)6-7-9(14)17-4/h8H,6-7H2,1-5H3,(H,13,16)/t8-/m0/s1

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59279-60-6 Process route

dimethyl (2S)-2-{N-[(tert-butoxy)carbonyl]benzyloxycarbonylamino}pentane-1,5-dioate
500143-66-8

dimethyl (2S)-2-{N-[(tert-butoxy)carbonyl]benzyloxycarbonylamino}pentane-1,5-dioate

dimethyl (S)-N-(benzyloxycarbonyl)glutamate
67436-17-3

dimethyl (S)-N-(benzyloxycarbonyl)glutamate

dimethyl (2S)-2-[(tert-butoxycarbonyl)amino]pentanedioate
59279-60-6,130622-05-8,861658-15-3

dimethyl (2S)-2-[(tert-butoxycarbonyl)amino]pentanedioate

Conditions
Conditions Yield
With lithium bromide; In acetonitrile; at 65 ℃; for 10h;
With lithium bromide; In acetonitrile; at 65 ℃; for 10h; Title compound not separated from byproducts.;
di-<i>tert</i>-butyl dicarbonate
24424-99-5

di-tert-butyl dicarbonate

L-glutamic dimethyl ester hydrochloride
23150-65-4

L-glutamic dimethyl ester hydrochloride

dimethyl (2S)-2-[(tert-butoxycarbonyl)amino]pentanedioate
59279-60-6,130622-05-8,861658-15-3

dimethyl (2S)-2-[(tert-butoxycarbonyl)amino]pentanedioate

Conditions
Conditions Yield
With sodium hydrogencarbonate; In tetrahydrofuran; water; at 20 ℃; for 16h; Inert atmosphere;
100%
With iodine; at 20 ℃; for 1h;
88%
With zirconium(IV) chloride; In acetonitrile; at 20 ℃; for 0.166667h;
80%
With triethylamine; dmap; In dichloromethane; at 0 - 20 ℃;
68%
With triethylamine; In methanol; for 18h;
With sodium carbonate; In water; ethyl acetate; at 20 ℃; for 18h;
With dmap; triethylamine; In 1,4-dioxane; water;
With triethylamine; In methanol; for 6h; Cooling with ice;
With triethylamine; In dichloromethane; at 0 - 20 ℃; for 10.25h; Inert atmosphere;
With sodium hydroxide; In water; ethyl acetate; for 12h; pH=9 - 10; Large scale;
843 g

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