Reacción #9188

ord-f75c4e99532d4a508cd22f8965bec48f

Ecuación de reacción

O=C(Cl)OCc1ccccc1
benzyl chloroformate
CCOC(=O)c1sc(N)nc1C
ethyl-2-amino-4-methyl-thiazole-5-carboxylate
O=C([O-])O.[Na+]
NaHCO3
O=C(Cl)OCc1ccccc1
Benzyl chloroformate
CCOC(=O)c1sc(NOC(=O)OCc2ccccc2)nc1C
title compound
Rendimiento 48.0%
CCOC(=O)c1sc(NOC(=O)OCc2ccccc2)nc1C
Ethyl-2-benzyloxycarbonyloxyamino-4-methyl-thiazole-5-carboxylate
Rendimiento 48.0%

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe organic layer was separated
  2. 2
    Secadodried (MgSO4)
  3. 3
    Filtraciónfiltered
  4. 4
    Concentraciónconcentrated
  5. 5
    OtroThe residue was chromatographed on a silica gel column
  6. 6
    LavadoElution with 10% EtOAc in hexanes

Procedimiento

A 3 M aq. NaHCO3 solution (10 mL, 30 mmol) was added to a stirred solution of ethyl-2-amino-4-methyl-thiazole-5-carboxylate (372 mg, 2 mmol) in THF (20 mL) at 0–5° C. Benzyl chloroformate (500 μL) was added. After 2 h, additional benzyl chloroformate (500 μL) and the biphasic solution was stirred for an additional 2 h at 0–5° C. The mixture was diluted with dichloromethane (50 mL) and water (30 mL). The organic layer was separated, dried (MgSO4), filtered and concentrated. The residue was chromatographed on a silica gel column. Elution with 10% EtOAc in hexanes followed by 20% and 30% EtOAc in hexanes afforded the title compound (310 mg, 48%) as a white solid.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07091223B2uspto-grants-2006_08