Réaction #4592

Équation de réaction

sodium cyanamide

DCC

N-hydroxysuccinimide

N-benzoyl-L-leucine

→

N-Benzoyl-L-leucylcyanamide

Rendement 42.9%

Solvants

THF

—

EtOAc petroleum ether THF CH2Cl2 AcOH

water

—

EtOAc petroleum ether AcOH

acetonitrile

Conditions de réaction

Traitement

1. 1
   FiltrationThe reaction mixture was filtered
2. 2
   Autreto remove the bulk of the DCU
3. 3
   Autrethe filtrate was evaporated in vacuo to dryness
4. 4
   workup.DISSOLUTIONThe resulting semi-solid residue was redissolved in THF
5. 5
   Filtrationthe mixture filtered
6. 6
   Autreto remove any residual DCU
7. 7
   AutreThe filtrate was evaporated in vacuo
8. 8
   Autreto give crude N-benzoyl-L-leucine N-hydroxysuccinimide ester as a foamy residue
9. 9
   workup.WAITto proceed at room temperature for 24 hours
10. 10
    ConcentrationThe reaction mixture was then concentrated in vacuo to half its original volume
11. 11
    Filtrationfiltered
12. 12
    ExtractionThe filtrate (pH 9) was extracted with ethyl acetate (2×50 ml)
13. 13
    AutreThe aqueous layer was separated
14. 14
    Extractionextracted with methylene chloride (3×50 ml)
15. 15
    ExtractionThe methylene chloride extract
16. 16
    Séchagewas dried over anhydrous sodium sulfate
17. 17
    Filtrationfiltered
18. 18
    AutreThe filtrate was evaporated in vacuo
19. 19
    Autreto give 2.80 g (92.4% yield) of crude product as a tacky white solid
20. 20
    AutreThis was triturated with diethyl ether
21. 21
    Autrecollected
22. 22
    Autreto give 1.30 g (42.9% yield of white powdery 11, mp 136°-137° C. [α]D23 +0.7°(c 1.0, CH3OH)
23. 23
    Autrequenching

Mode opératoire

DCC (2.41 g, 0.0117 mol) and N-hydroxysuccinimide (1.35 g, 0.0117 mol) were added to a solution of N-benzoyl-L-leucine (2.75 g, 0.0117 mol) in 100 ml of acetonitrile at ice bath temperature. The reaction was allowed to proceed at this temperature for 2 hours. The reaction mixture was filtered to remove the bulk of the DCU and the filtrate was evaporated in vacuo to dryness. The resulting semi-solid residue was redissolved in THF and the mixture filtered to remove any residual DCU. The filtrate was evaporated in vacuo to give crude N-benzoyl-L-leucine N-hydroxysuccinimide ester as a foamy residue. IR (neat, cm-1) 3340 NH), 3060 (C6H5), 1820, 1790, 1740 and 1650 (C=O); NMR (Silanor C, δ from TMS) 7.3-7.9 (m, C6H5), 5.1-5.3 (m, --NH--CH--C=O), 2.8 (s, cycl. --CH2 --CH2 --), 1.6-2.2 (m, CH--CH2 --), 0.9-1.1 (d, (CH3)3CH). This was dissolved in 100 ml of THF and added drop-wise to a solution of sodium cyanamide (1.50 g, 0.0234 mol) in 100 ml of distilled water at ice bath temperature. The reaction was allowed to proceed at room temperature for 24 hours. The reaction mixture was then concentrated in vacuo to half its original volume and filtered. The filtrate (pH 9) was extracted with ethyl acetate (2×50 ml). The aqueous layer was separated, acidified to pH 1.5 with 10% HCl, and extracted with methylene chloride (3×50 ml). The methylene chloride extract was dried over anhydrous sodium sulfate and filtered. The filtrate was evaporated in vacuo to give 2.80 g (92.4% yield) of crude product as a tacky white solid. This was triturated with diethyl ether and collected to give 1.30 g (42.9% yield of white powdery 11, mp 136°-137° C. [α]D23 +0.7°(c 1.0, CH3OH); TLC: Rf =0.93 in EtOAc/petroleum ether/THF/CH2Cl2 / AcOH (50:50:10:50:4) and 0.24 in EtOAc/petroleum ether/AcOH (50:100:1), detected by UV quenching and orange color with ferricyanide spray reagent; IR (Nujol, cm-1) 3300, 3100 (NH), 2230 (C≡N), 1750 and 1630 (C=O); NMR (Silanor-DMSO, δ from TMS) 7.4-8.0 (d, C6H5 --), 4.2-4.6 (m, --NH--CH--C=O), 1.4-1.9 (m, CH--CH2 --), 0.8-1.1 (d, (CH3)2CH--) Anal. Calcd for C14H17N3O2 : C, 64.85; H, 6.61; N, 16.20. Found C, 64.62; H, 6.73; N, 15.93.

Source