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N-(tert-butoxycarbonyl)glycine → Ethyl 2-(2-(2-aminoacetamido)thiazol-4-yl)acetate

HRID 1871975
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1871975
C(OC([NH:8][CH2:9][C:10](O)=[O:11])=O)(C)(C)C.[CH2:13]([O:15][C:16](=[O:24])[CH2:17][C:18]1[N:19]=[C:20]([NH2:23])[S:21][CH:22]=1)[CH3:14].F[P-](F)(F)(F)(F)F.Br[P+](N1CCCC1)(N1CCCC1)N1CCCC1.C(N(CC)C(C)C)(C)C>CN(C)C=O.CN(C1C=CN=CC=1)C>[NH2:8][CH2:9][C:10]([NH:23][C:20]1[S:21][CH:22]=[C:18]([CH2:17][C:16]([O:15][CH2:13][CH3:14])=[O:24])[N:19]=1)=[O:11]
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Komponenten

7

Edukt 4

HCID 78288N-(tert-butoxycarbonyl)glycineHCID 81531DiisopropylethylamineHCID 1044544-Thiazoleacetic acid, 2-amino-, ethyl esterHCID 2733179PyBroP

Produkt 1

HCID 54551034Ethyl 2-(2-(2-aminoacetamido)thiazol-4-yl)acetate

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 14284
4-(Dimethylamino)pyridine
Katalysator
HCID 6228DimethylformamideLösungsmittel

Versuchsvorschrift

A mixture of N-(tert-butoxycarbonyl)glycine (3.1 g), 2-amino-4-thiazoleacetic acid ethyl ester (3 g) and bromo-tris(pyrrolidino)-phosphonium hexafluorophosphate (7.54 g) in dimethylformamide (20 ml) was treated with N,N-diisopropylethylamine (6 ml). After 25 minutes N,N-dimethyl-4-aminopyridine (1.96 g) was added. After 24 hours the mixture was partitioned between ethyl acetate and brine. The organic phase was washed with saturated aqueous sodium bicarbonate, brine, IN HCl and brine, dried (MgSO4) and evaporated. The residue was purified by chromatography eluting with 50% ethyl acetate in isohexane. The product (0.77 g) was dissolved in dichloromethane (25 ml) and trifluoroacetic acid (10 ml). After 2 hours the mixture was evaporated. The residue was partitioned between ethyl acetate and sodium bicarbonate solution. The aqueous phase was repeatedly extracted with ethyl acetate. The combined extracts were dried (MgSO4) and evaporated. Yield 0.41 g.

Aufarbeitung

  1. customAfter 24 hours the mixture was partitioned between ethyl acetate and brine
  2. washThe organic phase was washed with saturated aqueous sodium bicarbonate, brine, IN HCl
  3. dry with materialbrine, dried (MgSO4)
  4. customevaporated
  5. customThe residue was purified by chromatography
  6. washeluting with 50% ethyl acetate in isohexane
  7. dissolutionThe product (0.77 g) was dissolved in dichloromethane (25 ml)
  8. customAfter 2 hours the mixture was evaporated
  9. customThe residue was partitioned between ethyl acetate and sodium bicarbonate solution
  10. extractionThe aqueous phase was repeatedly extracted with ethyl acetate
  11. dry with materialThe combined extracts were dried (MgSO4)
  12. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-5dbda3ddb30a486ba67918a915667c9a
Quelldatensatz
uspto-grants-2000_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06107297

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