Реакция #969841

ord-932596673fb048d0bdd30485884763dc

Уравнение реакции

CC#N
acetonitrile
O
water
[N-]=[N+]=NCCOCCOCCOCCN
11-azido-3,6,9-trioxaundecanamine
O=C1COCC(=O)O1
diglycolic anhydride
[N-]=[N+]=NCCOCCOCCOCCNC(=O)COCC(=O)O
yellow syrup
[N-]=[N+]=NCCOCCOCCOCCNC(=O)COCC(=O)O
17-Azido-5-oxo-6-aza-3,9,12,15-tetraoxaheptadecanoic acid

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.WAITgradient 4-16% B over 20 min
  2. 2
    КонцентрированиеThe solution was concentrated

Методика

To a solution of 11-azido-3,6,9-trioxaundecanamine (10.9 g, 50.0 mmol) in dichloromethane (100 ml) was added diglycolic anhydride (6.38 g, 55.0 mmol). The reaction mixture was stirred overnight. HPLC analysis (column Vydac 218TP54; solvents: A=water/0.1% TFA and B=acetonitrile/0.1% TFA; gradient 4-16% B over 20 min; flow 1.0 ml/min; UV detection at 214 and 284 nm), showed complete conversion of starting material to a product with retention time 18.3 min. The solution was concentrated to give quantitative yield of a yellow syrup. The product was analysed by LC-MS (ES ionisation) giving [MH]+ at 335 as expected. 1H (500 MHz) and 13C (125 MHz) NMR spectroscopy was in agreement with structure The product was used in the next step without further purification.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08236283B2uspto-grants-2012_08