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4-phenyl-3,4,5,6-tetrahydrobenzo[h]quinazoline-2(1H)-thione synthesis

7synthesis methods
-

Yield:85660-18-0 93%

Reaction Conditions:

with zinc aluminate in neat (no solvent) at 100; for 2 h;Milling;

Steps:

2.2.1. Products a,b and c

General procedure: A mixture of A/B or C (Schemes 1-2, 1 mmol) andmalononitrile/thiourea (1.2 mmol), and ZnAl2O4 (0.3 mmol)was milled in a stainless steel grinding vial (10 mL volume)equipped with a stainless steel ball (diameter: 6 mm; mass:1.04 g) for 0.6-1.5 h at 25 Hz and 100°C. After completionof the reaction which confirmed by TLC (eluent: nhexane/ethyl acetate: 4/1), the resulting crude productmixture was transferred with boiling ethanol for purification.The catalyst was filtered; and the solvent was evaporated.Then, the solid product was purified by recrystallizationprocedure in aqueous EtOH.

References:

Ghashang, Majid;Janghorban, Sadaf;Roudbaraki, Seyyed Jalal [Combinatorial chemistry and high throughput screening,2019,vol. 22,# 6,p. 421 - 427]