تفاعل #1771286

ord-9034fde3a9164a89af163dfcf8e9706e

معادلة التفاعل

O=C(Cl)CBr
bromoacetyl chloride
[Br-].[K+]
KBr
c1ccncc1
pyridine
CNC(=O)c1c(N)c(OC)c(C(=O)NC)c(N)c1OC
9
CNC(=O)c1c(N)c(OC)c(C(=O)NC)c(N)c1OC
3,6-Bis(methylcarbamyl)-1,4-dimethoxy-2,5-diaminobenzene
CN(C)C=O
dimethyl formamide
CNC(=O)c1c(NC(=O)CBr)c(OC)c(C(=O)NC)c(NC(=O)CBr)c1OC
2,5 -Bis(bromoacetamido)-3,6-bis(methylcarbamyl)-1,4-dimethoxybenzene

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    ترشيحthe precipitated product was filtered off
  2. 2
    غسيلrinsed with water
  3. 3
    غسيلrinsed with ethanol
  4. 4
    أخرى393 mg (53%) yield

الإجراء التجريبي

To a solution of 503 mg (1.42 mmol) of 9 .2HCl in 15 mL of dry dimethyl formamide were added sequentially, 533 μL (6.59 mmol) of pyridine and 282 μL (3.42 mmol) of bromoacetyl chloride. After allowing the mixture to stir at room temperature for 6 hours, the precipitated product was filtered off and rinsed with water and then rinsed with ethanol: 393 mg (53%) yield; mp 308°-310° C.; TLC (n-butanol/acetic acid/water [5:2:3]), Rf =0.58; IR (KBr pellet) 3380, 3278, 1681, 1638, 1551, 1472, 1411, 1325, 1238, 1047 cm-1 ; 1H NMR (dimethyl-d6 sulfoxide) δ9.72 (2H, s, 2- and 5-acetamido N(H), 7.87 (2H, brs, 3- and 6-carbamyl proton), 4.22 (4H, s, methylenes), 3.65 (6H, s, methoxys), 2.70 (6H, d, J=4.6 Hz, 3- and 6-carbamyl methyl); mass spectrum (EI mode) m/z 522, 524 and 526 (P+ for the 79Br, 79Br; 79Br, 81Br; 81Br, 81Br combinations, respectively, at an intensity ratio of 1:2:1).

المصدر

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