تفاعل #341447

ord-f7b642a9827045fba7662f51cdc3c5fe

معادلة التفاعل

O=C(Nc1cccc(CO)c1)N(CCC(c1ccccc1)c1ccccc1)CCN1CCOCC1
1-(3,3-diphenylpropyl)-3-(3-hydroxymethylphenyl)-1-(2-morpholin-4-ylethyl)urea
O=Cc1cccc(NC(=O)N(CCC(c2ccccc2)c2ccccc2)CCN2CCOCC2)c1
1-(3,3-diphenylpropyl)-3-(3-formylphenyl)-1-(2-morpholin-4-ylethyl)urea
المردود 84.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةThe mixture is heated
  2. 2
    درجة الحرارةunder reflux for one night
  3. 3
    ترشيحthe reaction medium is filtered over Celite®
  4. 4
    غسيلAfter rinsing with dichloromethane
  5. 5
    تركيزthen concentrating to dryness
  6. 6
    أخرىthe crude reaction product
  7. 7
    أخرىis purified by flash chromatography over silica gel (
  8. 8
    غسيلelution gradient

الإجراء التجريبي

105.2 mg (0.222 mmol, 1 eq.) of 1-(3,3-diphenylpropyl)-3-(3-hydroxymethylphenyl)-1-(2-morpholin-4-ylethyl)urea (obtained in Example 60), 6 mL of chloroform, and 193 mg (2.22 mmol, 10 eq.) of manganese oxide are introduced in succession into a 50 mL flask under an argon atmosphere while stirring. The mixture is heated under reflux for one night, then the reaction medium is filtered over Celite®. After rinsing with dichloromethane then concentrating to dryness, the crude reaction product is purified by flash chromatography over silica gel (elution gradient: CH2Cl2/AcOEt 4/1 then 1/1), leading to the desired aldehyde in a yield of 84%.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07875609B2uspto-grants-2011_01