Реакция #1435679

ord-9221c582fd7c48b4ab7edcc446b8038e

Уравнение реакции

CC(C)C[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)CNC(=O)OC(C)(C)C)C(=O)O
Boc-Gly-L-Phe-L-Leu-OH
CN(C)[P+](On1nnc2ccccc21)(N(C)C)N(C)C
benzotriazol-1-yloxytris(dimethylamino)phosphonium
CCN(C(C)C)C(C)C
DIEA
CC(C)C[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)CN)C(=O)O
Gly-L-Phe-L-Leu

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.ADDITIONcontaining amino derivatized ELAMS™
  2. 2
    ДругоеThe tube is sealed
  3. 3
    Промывкаwashed with DMF (3×) and methylene chloride (2×)
  4. 4
    workup.WAITThe ELAMS™ are then deprotected with a solution of 50% trifluoroacetic acid (TFA) in methylene chloride for 30 min.
  5. 5
    Промывкаwashed with methylene chloride (2×), ethanol (2×) and methylene chloride (2×)
  6. 6
    Другоеdried at 55° C. for about 1 hour

Методика

Boc-Gly-L-Phe-L-Leu-OH (44 mg, 0.1 mmol), benzotriazol-1-yloxytris(dimethylamino)phosphonium hexaflurophsophate (14 mg, 0.104 mmol) are dissolved in dry DMF (1 mL). DIEA (20 μL, 0.115 mmol) is added and about 0.5-1.0 mL of this solution is transferred to a test tube containing amino derivatized ELAMS™. The tube is sealed, vortexed for about 3.5-4 hours and the ELAMS™ pelleted and washed with DMF (3×) and methylene chloride (2×). The ELAMS™ are then deprotected with a solution of 50% trifluoroacetic acid (TFA) in methylene chloride for 30 min., washed with methylene chloride (2×), ethanol (2×) and methylene chloride (2×), and dried at 55° C. for about 1 hour. The identifier tag from each ELAMS™ is detected and recorded.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: USRE039606E1uspto-grants-2007_05