반응 #50426

ord-7dd6d28afe984fcabec32adca10aa985

반응 방정식

CCCN(CCC)C1CCc2cccc(C(=O)C=CN(C)C)c2C1
2-Di-n-propylamino-8-(1-oxo-3-(dimethylamino)-prop-2-enyl)-1,2,3,4-tetrahydronaphthalene
N=C(N)N
guanidine
CCCN(CCC)C1CCc2cccc(-c3ccnc(N)n3)c2C1
title compound
CCCN(CCC)C1CCc2cccc(-c3ccnc(N)n3)c2C1
2-Di-n-propylamino-8-(2-aminopyrimidin-4-yl)-1,2,3,4-tetrahydronaphthalene

용매

반응 조건

온도
60°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도The mixture then was cooled to room temperature during which a crystalline solid
  2. 2
    기타formed
  3. 3
    여과The crystals were filtered
  4. 4
    세척washed with isopropyl alcohol, ether
  5. 5
    기타dried in vacuo

실험 절차

2-Di-n-propylamino-8-(1-oxo-3-(dimethylamino)-prop-2-enyl)-1,2,3,4-tetrahydronaphthalene, prepared as in Example 8 (0.18 g; 0.55 mmol) was dissolved in 3 ml of ethanol. To the mixture was added 0.07 g (1.1 mmol) of guanidine, and the mixture was stirred at 60° C. under nitrogen for 18 hours. The mixture then was cooled to room temperature during which a crystalline solid formed. The crystals were filtered, washed with isopropyl alcohol, ether, and dried in vacuo to give 70 mg of the title compound as glistening plates. The product was recrystallized from isopropyl alcohol to obtain colorless crystals, m.p. 188°-189° C. Analysis: Theory: C, 74.04; H, 8.70; N, 17.27; Found: C, 74.30; H, 8.70; N, 17.45.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05426226uspto-grants-1995_06