تفاعل #61069

ord-056fb401bffd4356bf19d7e545d3779b

معادلة التفاعل

ClCCl
CH2Cl2
[N-]=C=O
isocyanate
Nc1cc[nH]n1
3-aminopyrazole
O=C=NCCCCl
3-chloropropyl isocyanate
CN(C)C=O
DMF
O=C(NCCCCl)Nc1ccn(C(=O)NCCCCl)n1
title compound
المردود 32.0%
O=C(NCCCCl)Nc1ccn(C(=O)NCCCCl)n1
N-(3-Chloropropyl)-3-({[(3-chloropropyl)amino]carbonyl}amino)-1H-pyrazole-1-carboxamide
المردود 32.0%

الكواشف

لا شيء

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGThe reaction mixture was stirred for an additional 48 hr
  2. 2
    أخرىNaCl and the phases were separated
  3. 3
    استخلاصThe aqueous layer was extracted with CH2Cl2 (2×20 mL)
  4. 4
    تجفيفthe combined organic extracts were dried over anh. Na2SO4
  5. 5
    ترشيحThe solids were filtered
  6. 6
    أخرىthe solvent evaporated
  7. 7
    أخرىThe crude product was purified by flash chromatography (Biotage 40, cHex/EtOAc 7:3)

الإجراء التجريبي

To a solution of 3-aminopyrazole (500 mg, 6 mmol), in anh. DMF (10 mL), at r.t., under N2, was added 3-chloropropyl isocyanate (1.2 mL, 2 eq) and the reaction was stirred for 24 hr. The reaction was not complete and more isocyanate (1.2 mL, 2 eq) was added. The reaction mixture was stirred for an additional 48 hr. It was then poured into CH2Cl2/sat.aq. NaCl and the phases were separated. The aqueous layer was extracted with CH2Cl2 (2×20 mL) and the combined organic extracts were dried over anh. Na2SO4. The solids were filtered and the solvent evaporated. The crude product was purified by flash chromatography (Biotage 40, cHex/EtOAc 7:3) to give the title compound as a white solid (620 mg, 32%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07427630B2uspto-grants-2008_09