Formaldehyde → Nepsilon-dimethylamino-Nalpha-CBZ-O-t-butyl L-lysine

HRID 1175

Reaktionsgleichung

Reaktionsgleichung von HRID 1175
[BH3-][C:2]#[N:3].[Na+].[C:5]([NH:15][C@H:16]([C:22]([O:24][C:25]([CH3:28])([CH3:27])[CH3:26])=[O:23])[CH2:17][CH2:18][CH2:19][CH2:20][NH2:21])([O:7][CH2:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)=[O:6].[CH2:29]=O>CO.[Cl-].[Cl-].[Zn+2]>[CH3:29][N:3]([CH3:2])[NH:21][CH2:20][CH2:19][CH2:18][CH2:17][C@@H:16]([C:22]([O:24][C:25]([CH3:28])([CH3:27])[CH3:26])=[O:23])[NH:15][C:5]([O:7][CH2:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)=[O:6]

Komponenten

6

Edukt 3

HCID 712FormaldehydeHCID 5003444Sodium cyanoborohydrideHCID 11078219N2-[(Phenylmethoxy)carbonyl]-L-lysine tert-Butyl Ester

Produkt 1

HCID 22883010Nepsilon-dimethylamino-Nalpha-CBZ-O-t-butyl L-lysine

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 3007855ZincchlorideKatalysatorHCID 887MethanolLösungsmittel2×

Versuchsvorschrift

A mixture consisting of 3.7 (27.2 mmol) of ZnCl2, 3.2 g (53 mmol) of NaCNBH3 and 60 mL of methanol was prepared to which was added a solution of 18 g (51.7 mmol) of the amine 1 in 180 mL of methanol. After cooling to 10°-15° C. 12.4 mL of 37% formaldehyde (165 mmol) was added dropwise over a 2-3 minute period. The reaction was stirred for 1 hour and monitored by silica gel TLC with elution using a 60:10:1(v/v/v/) mixture of chloroform/methanol/concentrated ammonia (solvent A). One hundred milliliters of water was added and the mixture concentrated to a volume of 200 ml. Ethyl acetate (200 mL) was added and the pH raised to 10.5 with 10% NaOH. The ethyl acetate was separated and the pH of the aqueous phase readjusted to 10.5 and extracted with 200 mL of fresh ethyl acetate. The ethyl acetate extracts were combined, washed with NaCl, dried over Na2SO4, filtered and concentrated to yield, after drying overnight under high vacuum, 14.86 g of viscous oil.

Aufarbeitung

  1. customwas prepared to which
  2. temperatureAfter cooling to 10°-15° C
  3. washmonitored by silica gel TLC with elution
  4. addition1(v/v/v/) mixture of chloroform/methanol/concentrated ammonia (solvent A)
  5. additionOne hundred milliliters of water was added
  6. concentrationthe mixture concentrated to a volume of 200 ml
  7. additionEthyl acetate (200 mL) was added
  8. temperaturethe pH raised to 10.5 with 10% NaOH
  9. customThe ethyl acetate was separated
  10. extractionextracted with 200 mL of fresh ethyl acetate
  11. washwashed with NaCl
  12. dry with materialdried over Na2SO4
  13. filtrationfiltered
  14. concentrationconcentrated
  15. customto yield
  16. dry with materialafter drying overnight under high vacuum, 14.86 g of viscous oil

Quellen und Nachweise

ORD-Eintrag
ord-fcbfd11331bc48daad13c3d9090822ab
Quelldatensatz
uspto-grants-1998_03
Patentnummer
US05723619

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