SU453833A3 - - Google Patents
Info
- Publication number
- SU453833A3 SU453833A3 SU1832412A SU1832412A SU453833A3 SU 453833 A3 SU453833 A3 SU 453833A3 SU 1832412 A SU1832412 A SU 1832412A SU 1832412 A SU1832412 A SU 1832412A SU 453833 A3 SU453833 A3 SU 453833A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- hydrogen
- chloroform
- free
- double bond
- halogenated hydrocarbon
- Prior art date
Links
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims description 16
- 238000000034 method Methods 0.000 claims description 11
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 claims description 4
- 229910000040 hydrogen fluoride Inorganic materials 0.000 claims description 4
- 150000003431 steroids Chemical class 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims 4
- 239000001257 hydrogen Substances 0.000 claims 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
- 150000008282 halocarbons Chemical class 0.000 claims 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical group [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 claims 2
- 239000002253 acid Substances 0.000 claims 1
- 125000003700 epoxy group Chemical group 0.000 claims 1
- KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical compound C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 claims 1
- 150000002431 hydrogen Chemical class 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- -1 isopropylidene dioxy Chemical group 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 150000002148 esters Chemical group 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 229910017604 nitric acid Inorganic materials 0.000 description 4
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 239000004593 Epoxy Chemical group 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- 239000002879 Lewis base Substances 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 150000007527 lewis bases Chemical class 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J71/00—Steroids in which the cyclopenta(a)hydrophenanthrene skeleton is condensed with a heterocyclic ring
- C07J71/0005—Oxygen-containing hetero ring
- C07J71/0026—Oxygen-containing hetero ring cyclic ketals
- C07J71/0031—Oxygen-containing hetero ring cyclic ketals at positions 16, 17
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J5/00—Normal steroids containing carbon, hydrogen, halogen or oxygen, substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane and substituted in position 21 by only one singly bound oxygen atom, i.e. only one oxygen bound to position 21 by a single bond
- C07J5/0046—Normal steroids containing carbon, hydrogen, halogen or oxygen, substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane and substituted in position 21 by only one singly bound oxygen atom, i.e. only one oxygen bound to position 21 by a single bond substituted in position 17 alfa
- C07J5/0053—Normal steroids containing carbon, hydrogen, halogen or oxygen, substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane and substituted in position 21 by only one singly bound oxygen atom, i.e. only one oxygen bound to position 21 by a single bond substituted in position 17 alfa not substituted in position 16
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J5/00—Normal steroids containing carbon, hydrogen, halogen or oxygen, substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane and substituted in position 21 by only one singly bound oxygen atom, i.e. only one oxygen bound to position 21 by a single bond
- C07J5/0046—Normal steroids containing carbon, hydrogen, halogen or oxygen, substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane and substituted in position 21 by only one singly bound oxygen atom, i.e. only one oxygen bound to position 21 by a single bond substituted in position 17 alfa
- C07J5/0061—Normal steroids containing carbon, hydrogen, halogen or oxygen, substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane and substituted in position 21 by only one singly bound oxygen atom, i.e. only one oxygen bound to position 21 by a single bond substituted in position 17 alfa substituted in position 16
- C07J5/0069—Normal steroids containing carbon, hydrogen, halogen or oxygen, substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane and substituted in position 21 by only one singly bound oxygen atom, i.e. only one oxygen bound to position 21 by a single bond substituted in position 17 alfa substituted in position 16 by a saturated or unsaturated hydrocarbon group
- C07J5/0076—Normal steroids containing carbon, hydrogen, halogen or oxygen, substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane and substituted in position 21 by only one singly bound oxygen atom, i.e. only one oxygen bound to position 21 by a single bond substituted in position 17 alfa substituted in position 16 by a saturated or unsaturated hydrocarbon group by an alkyl group
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Steroid Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| HURI000445 HU163145B (enExample) | 1971-09-23 | 1971-09-23 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU453833A3 true SU453833A3 (enExample) | 1974-12-15 |
Family
ID=11000875
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU1832412A SU453833A3 (enExample) | 1971-09-23 | 1972-09-22 |
Country Status (13)
| Country | Link |
|---|---|
| JP (1) | JPS5111624B2 (enExample) |
| AT (1) | AT330375B (enExample) |
| CA (1) | CA969927A (enExample) |
| CS (1) | CS164787B2 (enExample) |
| DD (1) | DD99162A5 (enExample) |
| DE (1) | DE2246203C3 (enExample) |
| FR (1) | FR2158823A5 (enExample) |
| HU (1) | HU163145B (enExample) |
| NL (1) | NL7212423A (enExample) |
| PL (1) | PL79455B1 (enExample) |
| SE (1) | SE385121B (enExample) |
| SU (1) | SU453833A3 (enExample) |
| YU (1) | YU35036B (enExample) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5707984A (en) * | 1995-12-08 | 1998-01-13 | G. D. Searle & Co. | Steroid nitrite/nitrate ester derivatives useful as anti-inflammatory drugs |
| US5792758A (en) * | 1995-12-08 | 1998-08-11 | G. D. Searle & Co. | Steroid nitrite ester derivatives useful as anti-inflammatory drugs |
| US5824669A (en) | 1996-03-22 | 1998-10-20 | Nitromed, Inc. | Nitrosated and nitrosylated compounds and compositions and their use for treating respiratory disorders |
| US5837698A (en) * | 1996-05-02 | 1998-11-17 | G. D. Searle & Co. | Steroid nitrite and nitrate ester derivatives useful as anti-inflammatory drugs |
-
1971
- 1971-09-23 HU HURI000445 patent/HU163145B/hu unknown
-
1972
- 1972-09-13 NL NL7212423A patent/NL7212423A/xx not_active Application Discontinuation
- 1972-09-13 AT AT783972A patent/AT330375B/de active
- 1972-09-15 DD DD16570272A patent/DD99162A5/xx unknown
- 1972-09-21 SE SE1221372A patent/SE385121B/xx unknown
- 1972-09-21 YU YU239672A patent/YU35036B/xx unknown
- 1972-09-21 CS CS644272A patent/CS164787B2/cs unknown
- 1972-09-21 JP JP9505072A patent/JPS5111624B2/ja not_active Expired
- 1972-09-21 FR FR7233548A patent/FR2158823A5/fr not_active Expired
- 1972-09-21 PL PL15785472A patent/PL79455B1/pl unknown
- 1972-09-22 SU SU1832412A patent/SU453833A3/ru active
- 1972-09-22 CA CA152,373A patent/CA969927A/en not_active Expired
- 1972-09-22 DE DE19722246203 patent/DE2246203C3/de not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| HU163145B (enExample) | 1973-06-28 |
| CS164787B2 (enExample) | 1975-11-28 |
| DD99162A5 (enExample) | 1973-07-20 |
| DE2246203B2 (de) | 1976-07-08 |
| ATA783972A (de) | 1975-09-15 |
| DE2246203C3 (de) | 1982-01-21 |
| SE385121B (sv) | 1976-06-08 |
| YU239672A (en) | 1979-12-31 |
| CA969927A (en) | 1975-06-24 |
| YU35036B (en) | 1980-06-30 |
| AT330375B (de) | 1976-06-25 |
| DE2246203A1 (de) | 1973-03-29 |
| JPS4839470A (enExample) | 1973-06-09 |
| FR2158823A5 (en) | 1973-06-15 |
| NL7212423A (enExample) | 1973-03-27 |
| JPS5111624B2 (enExample) | 1976-04-13 |
| PL79455B1 (en) | 1975-06-30 |
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