Altrenogest
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Altrenogest
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CAS No:
850-52-2
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Formula:
C21H26O2
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Chemical Name:
Altrenogest
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Synonyms:
Estra-4,9,11-trien-3-one,17-hydroxy-17-(2-propen-1-yl)-,(17β)-;Estra-4,9,11-trien-3-one,17α-allyl-17-hydroxy-;Estra-4,9,11-trien-3-one,17-hydroxy-17-(2-propenyl)-,(17β)-;(17β)-17-Hydroxy-17-(2-propen-1-yl)estra-4,9,11-trien-3-one;DRC 6246;Allyltrenbolone;R 2267;RU 2267;Altrenogest;Regumate;A 35957;Matrix;Matrix (progestogen)
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CAS No:
Description
Altrenogest(A35957; RU2267) is a progestogen structurally related to veterinary steroid trenbolone.Target: Progesterone ReceptorAltrenogest is a progestogen structurally related to veterinary steroid trenbolone. Treatment of embryo-recipient mares with altrenogest appears to be beneficial in extending the degree of donor-recipient synchrony required for successful embryo transfer. Altrenogest treatment also seems to be conductive to pregnancy maintenance in recipients experiencing luteal
Characteristics
37.3
4.27560
Slightly yellow powder
1.1±0.1 g/cm3
120 °C
495.6°C at 760 mmHg
210.1±21.3 °C
1.594
0-6°C
Flammable; burning produces irritating fumes
D20 -72° (c = 0.5 in ethanol)
Safety Information
3
KG7745000
Treasury is ventilated, low temperature and dry; stored separately from food materials
Altrenogest Use and Manufacturing
In a 2L reactor, 500 g of triene (4, 9, 11-triene-3, 17-dione) was added at 10 ° C, use 500 g of ethylene glycol dissolved, And 34 g of HC1 gas was added, The temperature was raised to 60 ° C for 10 h, To the room temperature, the solvent is distilled off. Add 2.5L tetrahydrofuran, cool to below _0 ° C, Slowly drop the newly prepared 187mL allyl magnesium bromide diethyl ether (lmol / L) in the reactor, 3h drop finished, rose to 60 ° C reaction 3h, down to -10 ° C below, 200 mL of water and 200 mL of concentrated hydrochloric acid were added dropwise, Adjust ΡΗ = 1-3, Heating up to 60 ° C, Stirring 5h, Separate the upper, Dried over anhydrous sodium sulfate, The solvent was concentrated to 100 mL, Placed below 5 ° C frozen, Slowly Crystalline Tetraenetrienone crude, ethyl acetate recrystallized about 375g tetraenual estrone. Yield 65percent.In a 21-reactor, At 25 ° (adding 50 (triphenylene) to 4, 9, 11-triene-3, 17-dione) With 50081 ethylene glycol dissolved, And 68 g of HC1 gas was added, The temperature was raised to 60 ° C for 10 h, Down to room temperature, The solvent is distilled off. 4 L of tetrahydrofuran was added, Down to below _0 ° C, Slowly drop the freshly prepared 374 mL allyl magnesium chloride diethyl ether (lmol / L) in a reaction kettle, 3h drops finished, Rose to 50 reactions 2h, Down to below 10 ° C, 200 mL of water and 200 mL of concentrated hydrochloric acid were added dropwise, Adjust ΡΗ = 1-3, Heating up to 60 ° C, Stirring 5h, Separate the upper, Dried over anhydrous sodium sulfate, The solvent was concentrated to 100 mL, Put 5 ° C below the frozen, slow crystallization of tetracene estrone crude, Ethyl acetate was recrystallized to about 347 g tetraenual estrone. Yield 60percent.
antineoplastic
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