Réaction #955907

ord-03d8f1b26f8440ff82d53190bfaf897f

Équation de réaction

Cl
HCl
COC(=N)CCCCCCC(=N)OC
Dimethylsuberimidate
N.N.O=C(O)C(O)C(O)C(O)C(O)C(=O)O
bis(hydrochloride)
N.N.O=C(O)C(O)C(O)C(O)C(O)C(=O)O
Mucic Acid Diamine
CSC
DMS
CSC.N.N.O=C(O)C(O)C(O)C(O)C(O)C(=O)O
Mucic Acid Diamine DMS

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    workup.DISSOLUTIONto dissolve the components
  2. 2
    AutreThis solution was then dialyzed with a 3500 MWCO dialysis membrane (Pierce pleated dialysis tubing) in ddH2O for 24 h
  3. 3
    Autreto give 49 mg of a white fluffy powder

Mode opératoire

A 1.5 mL eppendorff tube was charged with a solution of 85.5 mg (0.233 mmol) of the bis(hydrochloride) salt of Example 3 (3) in 0.8 mL of 0.1 M NaHCO3. Dimethylsuberimidate.2HCl (DMS, Pierce Chemical Co., 63.6 mg, 0.233 mmol) was added and the solution was vortexed and centrifuged to dissolve the components. The resulting mixture was stirred at room temperature for 15 h. The mixture was then diluted to 8 mL with water and the pH was brought to 4 with the addition of 1 N HCl. This solution was then dialyzed with a 3500 MWCO dialysis membrane (Pierce pleated dialysis tubing) in ddH2O for 24 h. The dialyzed solution was lyophilized to dryness to give 49 mg of a white fluffy powder. 1H NMR (500 MHz, dDMSO) δ 9.15 (bs), 7.92 (bs), 5.43 (bs), 4.58 (bs), 4.17 (bs), 3.82 (bs), 3.37 (bs), 3.28 (bs), 2.82 (bs), 2.41 (bs), 1.61 (bs), 1.28 (bs). 13C NMR (126 MHz, dDMSO) δ 174.88 (s, 1H), 168.38 (s, 1H), 71.45 (s, 4H), 71.22 (s, 3H), 42.34 (s, 2H), 36.96 (s, 3H), 32.74 (s, 3H), 28.09 (s, 4H), 26.90 (s, 4H). Mw [GPC]=2520, Mw/Mn=1.15.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08968714B2uspto-grants-2015_03