Reacción #657299

ord-42e83ebae56c4c8e96698fc97f18f7a2

Ecuación de reacción

C=CC1CC1(NC(=O)C1CC2CC1C(=O)O2)C(=O)OCC
3
C=CC1CC1(NC(=O)C1CC2CC1C(=O)O2)C(=O)OCC
1-[(3-Oxo-2-oxa-bicyclo[2.2.1]heptane-5-carbonyl)-amino]-2-vinyl-cyclopropane carboxylic acid ethyl ester
CCN(C(C)C)C(C)C
DIPEA
O
water
C=CC1CC1(NC(=O)C1CC(O)CC1C(=O)O)C(=O)OCC.CCN(C(C)C)C(C)C
2-(1-Ethoxycarbonyl-2-vinylcyclopropylcarbamoyl)-4-hydroxy-cyclopentane carboxylic acid diisopropylethylamine salt

Condiciones de reacción

Temperatura
40°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe reaction vessel was sealed
  2. 2
    workup.STIRRINGAfter 1 min of pre-stirring
  3. 3
    Otrothe reaction was irradiated for 40 min to a set temperature of 100° C
  4. 4
    Concentraciónthe transparent solution was concentrated in vacuo
  5. 5
    Otroto remove any residual water

Procedimiento

To a solution of 3 (800 mg, 2.73 mmol) in water (15 mL) in a 20 mL microwave reaction vessel was added DIPEA (1.2 mL, 6.8 mmol) and a stir bar. The reaction vessel was sealed and the immiscible slurry was shaken vigorously before insertion in the microwave oven cavity. After 1 min of pre-stirring, the reaction was irradiated for 40 min to a set temperature of 100° C. After cooling to 40° C., the transparent solution was concentrated in vacuo, and the residual brown oil co-evaporated 3 times with MeCN to remove any residual water. The crude product 4, in the form of a DIPEA salt, was immediately taken forward to the next step. LC/MS (Method A): tR=1.29 min, >95%, m/z (ESI+)=312 (MH+).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09023808B2uspto-grants-2015_05