반응 #1288

ord-64ae065485524aae852fadf8328767e1

반응 방정식

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

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도cooled to 0° C.
  2. 2
    workup.STIRRINGAfter stirring at 0° C. for 1 hour and at room temperature for 2 hours
  3. 3
    기타the mixture was partitioned between ethyl acetate and 0.5N hydrochloric acid
  4. 4
    추출subsequently extracted three times with ethyl acetate
  5. 5
    세척The pooled ethyl acetate extracts were washed in succession with water, saturated sodium bicarbonate, and brine
  6. 6
    건조dried (sodium sulfate)
  7. 7
    여과filtered
  8. 8
    기타to give 5.77 g

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05723457uspto-grants-1998_03