تفاعل #708945

ord-0c35635aa2a840e98d4bcbaa04fb2a84

معادلة التفاعل

Nc1ccc(CC(CN(CC(=O)O)CC(=O)O)N(CC(=O)O)CC(=O)O)cc1
5
Nc1ccc(CC(CN(CC(=O)O)CC(=O)O)N(CC(=O)O)CC(=O)O)cc1
1-(p-aminobenzyl)ethylenediaminetetraacetic acid
O=C1OC2(OC=C(c3ccccc3)C2=O)c2ccccc21
fluorescamine
S=C(Cl)Cl
thiophosgene
O=C([O-])O.[Na+]
NaHCO3
O=C(O)CN(CC(=O)O)CC(Cc1ccc(N=C=S)cc1)N(CC(=O)O)CC(=O)O
1-(p-isothiocyanatobenzyl)ethylenediaminetetraacetic acid

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىfitted with an addition funnel
  2. 2
    workup.ADDITIONwas added dropwise
  3. 3
    workup.STIRRINGStirring
  4. 4
    أخرىPurification
  5. 5
    غسيلeluted with acetonitrile:water (30:8)
  6. 6
    غسيلThe product eluted from the column cleanly
  7. 7
    أخرىre-purified immediately

الإجراء التجريبي

The precursor 5 (0.33 mmol) was taken up in H2O (10 ml) and stirred rapidly in a 10 ml round bottom flask fitted with an addition funnel. The pH was adjusted to 8.5 with solid NaHCO3 and thiophosgene (42 mg, 0.365 mmol) in CHCl3 (10 ml) was added dropwise. Stirring was continued until the solution tested negative for amine by the fluorescamine method. The aqueous layer was taken to dryness. Purification was done by column chromatography on a 1×30 cm Florisil™ column eluted with acetonitrile:water (30:8). The product eluted from the column cleanly as determined by TLC and was stored in a dessicator in a freezer and re-purified immediately prior to use.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04824986uspto-grants-1989_04