反应详情

A solution of 1.75 g of N-(tert-butyl)-N′-[(1R)-1-hydroxymethyl-2-(4-thiazolyl)ethyl]thiourea in 20 cm3 of 6N hydrochloric acid is heated at a temperature in the region of 110° C. for 20 hours. The reaction medium is concentrated under reduced pressure (1 kPa) at a temperature in the region of 60° C., taken up in 5 cm3 of ethanol and then concentrated under the same conditions as above. The residue is taken up in 5 cm3 of ethanol and the product is then filtered off and dried in a desiccator under reduced pressure (0.1 kPa) at a temperature in the region of 40° C. 0.54 g of (+)-(4R)-4-(4-thiazolylmethyl)-4,5-dihydro-2-thiazolylamine dihydrochloride is obtained in the form of a cream-colored solid melting at 195° C. [1H NMR spectrum (300 MHz, (CD3)2SO-d6, δ in ppm): 3.67 (mt: 2H); 3.41 (dd, J=11.5 and 5.5 Hz: 1H); 3.68 (dd, J=11.5 and 8 Hz: 1H); 4.63 (mt: 1H); 7.59 (d, J=2 Hz: 1H); 9.14 (d, J=2 Hz: 1H); 9.18 (unresolved complex: 1H); 9.66 (unresolved complex: 1H); 10.04 (broad s: 1H); (αD20=+24.2+/−0.8 at a concentration of 0.5% in methanol)].

1. concentrationThe reaction medium is concentrated under reduced pressure (1 kPa) at a temperature in the region of 60° C.
2. concentrationconcentrated under the same conditions as above
3. filtrationthe product is then filtered off
4. customdried in a desiccator under reduced pressure (0.1 kPa) at a temperature in the region of 40° C