تفاعل #1771284

ord-0ce12021a1e543cd8ca80c1b9c5a81c1

معادلة التفاعل

COc1c(C(N)=O)c([N+](=O)[O-])c(OC)c(C(N)=O)c1[N+](=O)[O-]
6
COc1c(C(N)=O)c([N+](=O)[O-])c(OC)c(C(N)=O)c1[N+](=O)[O-]
3,6-Dicarbamyl-l,4-dimethoxy-2,5-dinitrobenzene
CO
methanol
Cl
hydrochloric acid
COc1c(N)c(C(N)=O)c(OC)c(N)c1C(N)=O
3,6-Dicarbamyl-1,4-dimethoxy-2,5-diaminobenzene

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONwas added immediately to the reaction mixture
  2. 2
    workup.STIRRINGwith stirring
  3. 3
    ترشيحAfter filtering the acidified mixture through CELITE
  4. 4
    غسيلwashing with methanol
  5. 5
    أخرىthe solvents were evaporated in vacuo
  6. 6
    أخرىthe solid residue thoroughly dried
  7. 7
    أخرىThe 8·2HCl was purified by dissolution in a minimum amount of hot methanol
  8. 8
    workup.ADDITIONfollowed by addition of ethyl acetate
  9. 9
    أخرى568 mg (97%) yield

الإجراء التجريبي

A mixture consisting of 561 mg (1.79 mmol) of 6, 50 mg of 5% Pd/C, and 100 mL of methanol was shaken under 50 psi of H2 for 4 hours. Upon completing the reduction, 10 mL of concentrated hydrochloric acid was added immediately to the reaction mixture with stirring. After filtering the acidified mixture through CELITE and washing with methanol, the solvents were evaporated in vacuo and the solid residue thoroughly dried. The 8·2HCl was purified by dissolution in a minimum amount of hot methanol followed by addition of ethyl acetate: 568 mg (97%) yield; TLC (n-butanol/acetic acid/water [5:2:3]), Rf =0.37; 1H NMR (dimethyl-d6 sulfoxide) δ7.93 and 7.92 (4H, 2 brs, 3- and 6-carbamyls, no assignments made), 3.69 (6H, s, methoxys); mass spectrum (EI mode), m/z 254 (P+).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05639881uspto-grants-1997_06