Reacción #1422

ord-32b402f60fe74c78b310c537e44ff646

Ecuación de reacción

CCOC(=O)CN.Cl
glycine, ethyl ester, hydrochloride salt
CN1CCOCC1
4-methyl morpholine
O=C(O)[C@H](CCCCO)N1C(=O)c2ccccc2C1=O
(S)-2-phthalimido-6-hydroxyhexanoic acid
Oc1cccc2[nH]nnc12
hydroxybenzotriazole
CCCC[C@@H](C(=O)NCC(=O)OCC)N1C(=O)c2ccccc2C1=O
title product
CCCC[C@@H](C(=O)NCC(=O)OCC)N1C(=O)c2ccccc2C1=O
(S)-N-(2-Phthalimido-1-oxohexyl)glycine, ethyl ester

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturacooled to 0° C.
  2. 2
    workup.STIRRINGAfter stirring at 0° C. for 1 hour and at room temperature for 2 hours
  3. 3
    Otrothe mixture was partitioned between ethyl acetate and 0.5N hydrochloric acid
  4. 4
    Extracciónsubsequently extracted three times with ethyl acetate
  5. 5
    LavadoThe pooled ethyl acetate extracts were washed in succession with water, saturated sodium bicarbonate, and brine
  6. 6
    Secadodried (sodium sulfate)
  7. 7
    Filtraciónfiltered
  8. 8
    Otroto give 5.77 g

Procedimiento

A slurry of glycine, ethyl ester, hydrochloride salt (2.718 g, 19.5 mmol.) in dimethylformamide (36 ml.) was treated with 4-methyl morpholine (2.60 ml., 2.39 g., 23.6 mmol.) and stirred at room temperature for 5 minutes. The mixture was then treated with (S)-2-phthalimido-6-hydroxyhexanoic acid (4.50 g., 16.2 mmol.) and hydroxybenzotriazole (2.225 g., 16.5 mmol.), cooled to 0° C., and then treated with ethyl-3-(3-dimethylamino)propyl carbodiimide, hydrochloride salt (3.438 g., 17.9 mmol.). After stirring at 0° C. for 1 hour and at room temperature for 2 hours, the mixture was partitioned between ethyl acetate and 0.5N hydrochloric acid and subsequently extracted three times with ethyl acetate. The pooled ethyl acetate extracts were washed in succession with water, saturated sodium bicarbonate, and brine, then dried (sodium sulfate), filtered and stripped to give 5.77 g. of title product as a colorless oil. TLC (ethyl acetate) Rf =0.34.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05723602uspto-grants-1998_03