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ChemicalBook CAS DataBase List 4-(4-cyclopropylnaphthalen-1-yl)-1H-1,2,4-triazole-5(4H)-thione

4-(4-cyclopropylnaphthalen-1-yl)-1H-1,2,4-triazole-5(4H)-thione synthesis

11synthesis methods
-

Yield: 90%

Reaction Conditions:

with water;sodium hydroxide in N,N-dimethyl-formamide at 30; for 16 h;Solvent;Temperature;Reagent/catalyst;

Steps:

5 Example 5. Preparation of 4-(4-cyclopropylnaphthalen-l-yl)-4H-l,2,4-triazole-3-thiol
Example 5. Preparation of 4-(4-cyclopropylnaphthalen-l-yl)-4H-l,2,4-triazole-3-thiol [070] To a round bottom flask added 4-(4-cyclopropyl-naphthalen-l-yl) -1-formylamino-thiourea (64.0 g, 225 mmol), DMF (300 mL) and 1 mol/L aqueous sodium hydroxide solution (225 mL) to form a mixture, the mixture was heated to about 30°C after stirred for about 16 hours, the mixture was cooled to room temperature (about 20°C). 1 mol/L hydrochloric acid (about 200 mL) was added into the mixture until the pH value of the mixture was about 6.0, then water (about 500 mL) was added. The mixture was stirred for about 15 minutes and filtered. The filter cake was washed with water, and the product was dried in vacuum at about 50°C for about 5 hours to obtain gray-green solid 4-(4-cyclopropylnaphthalen-l-yl)-4H-l,2,4-triazole-3 -thiol, 54.0 g, yield 90%. LC-Ms: m/z (ESI): 268(M+H)+, 1H MR (400 MHz, acetone-d6): δ 8.57 (d, J=8.0 Hz, 1 H), 8.37 (s, 1 H), 7.67 (m, 1 H), 7.60(m, 1 H), 7.5 l(d, J=8.0 Hz, 1 H), 7.48 (d, J=8.0 Hz, 1 H), 7.43 (d, J=8.0 Hz, 1 H), 2.50 (m, 1 H), 1.16 (m, 2 H), 0.84 (m, 2 H).

References:

SUNSHINE LAKE PHARMA CO., LTD.;CHEN, Weiqiang;LUO, Jian;LIU, Lixue;FAN, Yuping WO2014/198241, 2014, A1 Location in patent:Paragraph 069-070

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