Triethylamine → HCID 13132284, compound

HRID 2372578Notes

Reaction equation

HRID 2372578 reaction equation
[C:1]([NH:11][C@H:12]([C:14]([OH:16])=O)[CH3:13])([O:3][CH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)=[O:2].C(N(CC)CC)C.C(Cl)(=O)OCC(C)C.Cl.C([O:35][C:36](=[O:48])[CH2:37][NH:38][CH:39]1[CH2:47][C:46]2[C:41](=[CH:42][CH:43]=[CH:44][CH:45]=2)[CH2:40]1)C>O1CCCC1.C(Cl)(Cl)Cl>[C:1]([NH:11][C@H:12]([C:14]([N:38]([CH:39]1[CH2:47][C:46]2[C:41](=[CH:42][CH:43]=[CH:44][CH:45]=2)[CH2:40]1)[CH2:37][C:36]([OH:48])=[O:35])=[O:16])[CH3:13])([O:3][CH2:4][C:5]1[CH:6]=[CH:7][CH:8]=[CH:9][CH:10]=1)=[O:2]

Participants

7

Reactant 4

HCID 8471Triethylamine2×HCID 62365Isobutyl chloroformateHCID 736104N-carbobenzyloxyalanineHCID 13132277HCID 13132277, compound

Product 1

HCID 13132284HCID 13132284, compoundYield 66.9%

Reagents, catalysts & solvents 2

HCID 6212ChloroformSolventHCID 8028TetrahydrofuranSolvent

Procedure

A solution of 22.3 g of N-carbobenzoxy-L-alanine and 14 ml of triethylamine in 200 ml of tetrahydrofuran is cooled to -10° C., and 13.1 ml of isobutyl chlorocarbonate is added dropwise in portions with stirring. After stirring for 30 minutes, a solution of 24.1 g of N-(indan-2-yl)glycine ethyl ester hydrochloride and 14 ml of triethylamine in 200 ml of chloroform is added dropwise at -10° C. to -5° C. After standing overnight at room temperature, the reaction mixture is washed in sequence with water, aqueous sodium hydrogen carbonate, 10% hyrochloric acid and water, and dried over anhydrous sodium sulfate. The solvent is distilled off under reduced pressure, the residue is dissolved in 100 ml of methanol, 75 ml of 2 N sodium hydroxide is added, and the mixture is stirred at room temperature for 2 hours. Then, the mixture is made acidic with 10% hydrochloric acid to separate the resulting oil, which is extracted with 500 ml of ethyl acetate. The extract washed with water and dried, and the solvent is distilled off under reduced pressure to give 25 g of N-carbobenzoxy-L-alanyl-N-(indan-2-yl)glycine as an oil. This is dissolved in 50% ethanol and subjected to catalytic reduction in the presence of 4 g of 10% palladium-carbon. When the hydrogen absorption has ceased, the catalyst is filtered off, and the filtrate is concentrated under reduced pressure. Addition of 50 ml of methanol to the residue yields 11 g of L-alanyl-N-(indan-2-yl)glycine as colorless needles melting at 180°-182° C.

Workup

  1. stirringAfter stirring for 30 minutes
  2. washthe reaction mixture is washed in sequence with water, aqueous sodium hydrogen carbonate, 10% hyrochloric acid and water
  3. dry with materialdried over anhydrous sodium sulfate
  4. distillationThe solvent is distilled off under reduced pressure
  5. dissolutionthe residue is dissolved in 100 ml of methanol
  6. addition75 ml of 2 N sodium hydroxide is added
  7. stirringthe mixture is stirred at room temperature for 2 hours
  8. customto separate the resulting oil, which
  9. extractionis extracted with 500 ml of ethyl acetate
  10. washThe extract washed with water
  11. customdried
  12. distillationthe solvent is distilled off under reduced pressure

Sources & evidence

ORD record
ord-ed792e5135044205af836d58808b0733
Source dataset
uspto-grants-1992_03
Patent number
US05098892

Reaction notes

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