تفاعل #47898

ord-ef5a0690710f4457bbda238862f33705

معادلة التفاعل

CC(=O)O
acetic acid
CCOC(=O)C1CN(Cc2ccccc2)CCC1=O.Cl
ethyl 1-benzyl-4-oxopiperidine-3-carboxylate hydrochloride
CC(=O)O.N=CN
formamidine acetate
C[O-].[Na+]
sodium methoxide
O=c1[nH]cnc2c1CN(Cc1ccccc1)CC2
title compound
O=c1[nH]cnc2c1CN(Cc1ccccc1)CC2
6-Benzyl-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-4(3H)-one

المذيبات

ظروف التفاعل

درجة الحرارة
85°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىsealed
  2. 2
    أخرىreaction vessel
  3. 3
    درجة الحرارةto cool
  4. 4
    workup.ADDITIONpoured over ice
  5. 5
    أخرىa tan solid precipitated out
  6. 6
    ترشيحthe solid was filtered
  7. 7
    غسيلwashed with water and cold ether
  8. 8
    أخرىdried on high vacuum

الإجراء التجريبي

A mixture of ethyl 1-benzyl-4-oxopiperidine-3-carboxylate hydrochloride (50.0 g, 0.168 mol), formamidine acetate (16.2 g, 0.201 mol), 4.37 M of sodium methoxide in methanol (190 mL) and methanol (200 mL, 5 mol) was heated to 85° C. for 16 hour in a 350 ml sealed reaction vessel. The mixture was allowed to cool and reduced in vacuo. The residue was dissolved in 1N NaOH (150 ml) and poured over ice. Glacial acetic acid was added to the mixture until the pH of the mixture was 7 and a tan solid precipitated out. the solid was filtered, washed with water and cold ether, and dried on high vacuum to yield the title compound as a tan solid. (26.2 g, 61.4%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07745451B2uspto-grants-2010_06