Reacción #2175445

ord-d0bd5ae415fb49bf9039f39811c03c13

Ecuación de reacción

[N-]=[N+]=NCCOCCOCCOCCOCCOCCOCCOCCO
23-azido-3,6,9,12,15,18,21-heptaoxatricosan-1-ol
Cc1ccccc1S(=O)(=O)Cl
toluenesulfonyl chloride
c1ccncc1
pyridine
c1ccncc1
pyridine
Cc1ccc(S(=O)(=O)OCCOCCOCCOCCOCCOCCOCCOCCN=[N+]=[N-])cc1
3
Rendimiento 25.0%
Cc1ccc(S(=O)(=O)OCCOCCOCCOCCOCCOCCOCCOCCN=[N+]=[N-])cc1
23-azido-3,6,9,12,15,18,21-heptaoxatricos-1-yl p-toluenesulfonate
Rendimiento 25.0%

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe solvent was evaporated
  2. 2
    Otrothe crude product was purified on SiO2 column
  3. 3
    Otropurified on semipreparative HPLC (System E)

Procedimiento

A solution of 23-azido-3,6,9,12,15,18,21-heptaoxatricosan-1-ol (800 mg, 2.02 mmol) in pyridine (4 mL) was added dropwise to the solution of toluenesulfonyl chloride (771 mg, 4.04 mmol) and 4-dimethylaminopyridine (100 mg) in pyridine (10 mL) at room temperature. The mixture was stirred for 24 hours at room temperature. The solvent was evaporated and the crude product was purified on SiO2 column using hexanes/ethylacetate gradient 0-100% followed by ethylacetate/methanol gradient 0-100%, then purified on semipreparative HPLC (System E) to yield 280 mg (25%) of 3 as a colorless oil. 1H NMR (400 MHz, CDCl3): δ 2.45 (s, 3H), 3.38 (t, J=5.02 Hz, 2H), 3.58-3.70 (m, 28H), 4.16 (t, J=5.00 Hz, 2H), 7.34 (d, J=8.4 Hz, 2H), 7.80 (d, J=8.4 Hz, 2H); 13C NMR (100.6 MHz, CDCl3): δ 21.6, 50.7, 68.7, 69.2, 70.0, 70.5-70.8, 128.0, 129.7, 133.1, 144.7; MS ESI (m/z): [M+H]+ calcd. for C23H39N3O10S 549.24; found 549.9.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08435488B2uspto-grants-2013_05