تفاعل #2175442

ord-2457483880b444c0910fdf6f5b11f9b0

معادلة التفاعل

CC(C)N=C=NC(C)C
Diisopropylcarbodiimide
O=C(O)COc1ccc(COc2ccc(C(=O)c3cc(Cl)ccc3NC(=O)OCc3cccc4c3Cc3ccccc3-4)cc2)cc1
4-(4-(5-chloro-2-fluorenylmethoxycarbonylamino-benzoyl)-phenoxymethyl)phen oxyacetic acid
O.Oc1cccc2[nH]nnc12
hydroxybenzotriazole monohydrate
O=C1c2ccccc2C(=O)C1(O)O
ninhydrin
Nc1ccccc1C(=O)c1ccccc1
2-Aminobenzophenone

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.WAITvortexed for 24 hours at which point
  2. 2
    ترشيحThe solvent and reagents were filtered away from the solid support
  3. 3
    غسيلthe support was rinsed five times with 20 mL DMF and five times with 20 mL CH2Cl2 (for
  4. 4
    غسيلeach rinse the mixture
  5. 5
    workup.WAITwas vortexed for at least 30 seconds
  6. 6
    ترشيحbefore filtering off the solvent) and
  7. 7
    أخرىthen dried in vacuo for 12 hours
  8. 8
    أخرىto give 5

الإجراء التجريبي

To a 30 mL peptide reaction flask was added 4-(4-(5-chloro-2-fluorenylmethoxycarbonylamino-benzoyl)-phenoxymethyl)phen oxyacetic acid (1.52 g, 2.4 mmol, 2.0 equivalents), aminomethyl resin (1.99 g, 1.19 mmol of 1% crosslinked divinylbenzene-styrene, 100 mesh size, substitution level 0.60 milliequivalents/g), and hydroxybenzotriazole monohydrate (0.808 g, 5.28 mmol, 4.4 equivalents). Anhydrous DMF (12 mL) was added to the flask and the mixture was vortexed for 0.5 hour to fully solvate the resin. Diisopropylcarbodiimide (808 mg, 5.28 mmol, 4.4 equivalents) was added by syringe. The reaction flask was stoppered and then vortexed for 24 hours at which point the ninhydrin test on approximately 10 mg of the solid support demonstrated that coupling was complete. The solvent and reagents were filtered away from the solid support and the support was rinsed five times with 20 mL DMF and five times with 20 mL CH2Cl2 (for each rinse the mixture was vortexed for at least 30 seconds before filtering off the solvent) and then dried in vacuo for 12 hours to give 5.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08435492B2uspto-grants-2013_05