تفاعل #3541

ord-6a90e5dbf8d9440f860586cc73a69716

معادلة التفاعل

Nc1ncc2cc(-c3c(Cl)cccc3Cl)c(N)nc2n1
2,7-diamino-6-(2,6-dichlorophenyl)-pyrido[2,3-d]pyrimidine
NS(=O)(=O)O
sulfamic acid
CCN(CC)CCN
diethylaminoethylamine
CCN(CC)CCNc1ncc2cc(-c3c(Cl)cccc3Cl)c(N)nc2n1
6-(2,6-dichlorophenyl)-N2 -(2-diethylamino-ethyl)-pyrido[2,3-d]pyrimidine-2,7-diamine
N
NH3
المردود 1.0%

ظروف التفاعل

درجة الحرارة
150°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe excess diethylaminoethylamine was removed in vacuo
  2. 2
    workup.DISSOLUTIONThe resulting oil was dissolved in diethyl ether
  3. 3
    workup.ADDITIONdiluted with hexane
  4. 4
    ترشيحfiltered
  5. 5
    workup.DISSOLUTIONThe resulting solid was dissolved in dichloromethane which
  6. 6
    غسيلwas washed several times with water
  7. 7
    تجفيفdried with magnesium sulfate
  8. 8
    تركيزconcentrated in vacuo
  9. 9
    أخرىThe residue was crystallized from ethyl acetate

الإجراء التجريبي

A mixture of 2,7-diamino-6-(2,6-dichlorophenyl)-pyrido[2,3-d]pyrimidine (4.0 g) from Example 1, sulfamic acid (2.53 g), and diethylaminoethylamine (40 mL) was heated to approximately 150° C. for 20 hours. The excess diethylaminoethylamine was removed in vacuo. The resulting oil was dissolved in diethyl ether, diluted with hexane, and then filtered. The resulting solid was dissolved in dichloromethane which was washed several times with water, dried with magnesium sulfate, and concentrated in vacuo. The residue was crystallized from ethyl acetate to give the title compound 6-(2,6-dichlorophenyl)-N2 -(2-diethylamino-ethyl)-pyrido[2,3-d]pyrimidine-2,7-diamine, CIMS (1% NH3 in CH4): 433=M+ +C2H5, 405=M+ +H, 389=M+ -Et, 360; mp 216°-219.5° C.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05733913uspto-grants-1998_03