hydrocortamate hydrochloride

Originator

Magnacort,Pfizer,US,1956

Manufacturing Process

1 g of hydrocortisone is introduced with stirring into 5 cc of anhydrous pyridine. After heating to 45°C and then cooling again to 0°C to 5°C there is slowly added dropwise a freshly prepared solution of 0.52 g (1 mol + 10%) of chloracetic anhydride in 4 cc of absolute ether, The reaction temperature should not exceed 10°C. During the whole time of reaction a stream of nitrogen is passed through the reaction mixture in order to achieve an exhaustive evaporation of the added ether. The batch is slowly allowed to come to room temperature, an operation requiring 4 to 5 hours, and then 0.1 cc of water is added for decomposition of the excess of anhydride. The reaction solution is introduced dropwise with stirrinq within 1 hour into 100 cc of water as a result of which the 21-chloracetate of hydrocortisone is deposited. After filtration with suction, washing is carried out with water, 5% hydrochloric acid, water, 2% sodium bicarbonate solution and water again. The substance is then dried in a vacuum desiccator. The white chloracetate thus obtained melts at 213°C to 214°C with decomposition. It is free from nitrogen and the yield amounts to 93.4% of the theoretical.
1 g of hydrocortisone-21-chloracetate is dissolved in 15 cc of anhydrous and peroxide-free tetrahydrofuran. The solution produced is treated with a solution of 0.42 g of diethylamine in 15 cc of tetrahydrofuran. The reaction mixture is allowed to stand for 24 hours at room temperature. The separated diethylamine hydrochloride is filtered with suction and the filtrate evaporated under vacuum in a nitrogen atmosphere at 40°C. The residue is triturated with a little absolute ether and suction filtered. It is washed on the filter with a little ether and then with hexane. The 21-diethylaminoacetate of hydrocortisone melts at 150°C to 162°C. The base can be recrystallized from ethyl acetate but its melting point remains practically unchanged at 162°C to 163°C. The yield amounts to 72.5% of the theoretical. For conversion of the base into the hydrochloride it is suspended in ether and the suspension treated with ethereal hydrochloric acid. The hydrochloride is filtered with suction and recrystallized from ethanol; MP 222°C with decomposition.
With a starting quantity of 14g, the yield amounted to 85.4% of the theoretical.

brand name

Magnacort (Pfizer).

Therapeutic Function

Corticosteroid