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25985-08-4

Carbamimidothioicacid, (4-methoxyphenyl)methyl ester, hydrochloride (1:1) synthesis

5synthesis methods
-

Yield:25985-08-4 96%

Reaction Conditions:

with thiourea in tetrahydrofuran;

Steps:

a Dihydropyrimidine Intermediates

a. 2-(4-METHOXYBENZYL)-2-THIOPSEUDOUREA HYDROCHLORIDE. Into a well-stirred suspension of thiourea (7.6 g, 0.1 mol) in THF (50 mL) at 0° C., 4-methoxybenzyl chloride (16 g, 0.1 mol) was added in 10 min and the reaction mixture was allowed to warm to room temperature. After 2 hours the reaction mixture was heated to 65° C. and kept at that temperature for 5 hours. The reaction mixture was cooled to room temperature and diluted with diethyl ether (200 mL). The white precipitate that formed was filtered and dried (22.5 g, 96% yield); m. p. 161-163° C.

References:

US2003/69261,2003,A1

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