GB1005649A - A sulphur-containing derivative of vitamin b and processes for its manufacture - Google Patents
A sulphur-containing derivative of vitamin b and processes for its manufactureInfo
- Publication number
- GB1005649A GB1005649A GB866/64A GB86664A GB1005649A GB 1005649 A GB1005649 A GB 1005649A GB 866/64 A GB866/64 A GB 866/64A GB 86664 A GB86664 A GB 86664A GB 1005649 A GB1005649 A GB 1005649A
- Authority
- GB
- United Kingdom
- Prior art keywords
- disulphide
- pyridoxalyl
- reacting
- formula
- compound
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 title 1
- 239000005864 Sulphur Substances 0.000 title 1
- 238000004519 manufacturing process Methods 0.000 title 1
- 238000000034 method Methods 0.000 title 1
- 229940088594 vitamin Drugs 0.000 title 1
- 229930003231 vitamin Natural products 0.000 title 1
- 235000013343 vitamin Nutrition 0.000 title 1
- 239000011782 vitamin Substances 0.000 title 1
- 150000003722 vitamin derivatives Chemical class 0.000 title 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 8
- 150000001875 compounds Chemical class 0.000 abstract 4
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 abstract 3
- NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Chemical compound O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 abstract 3
- 125000003172 aldehyde group Chemical group 0.000 abstract 2
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 abstract 2
- MCIDYUGTJBLEST-UHFFFAOYSA-N 2,3-dinitrobenzaldehyde Chemical compound [O-][N+](=O)C1=CC=CC(C=O)=C1[N+]([O-])=O MCIDYUGTJBLEST-UHFFFAOYSA-N 0.000 abstract 1
- PEUVIOZMKDYCBM-UHFFFAOYSA-N 5-(chloromethyl)-3-hydroxy-2-methylpyridine-4-carbaldehyde Chemical compound ClCC=1C=NC(=C(C1C=O)O)C PEUVIOZMKDYCBM-UHFFFAOYSA-N 0.000 abstract 1
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 abstract 1
- 229920002472 Starch Polymers 0.000 abstract 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 abstract 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 abstract 1
- 150000001241 acetals Chemical class 0.000 abstract 1
- 230000002378 acidificating effect Effects 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 239000008101 lactose Substances 0.000 abstract 1
- 235000019359 magnesium stearate Nutrition 0.000 abstract 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 abstract 1
- JGOAZQAXRONCCI-SDNWHVSQSA-N n-[(e)-benzylideneamino]aniline Chemical compound C=1C=CC=CC=1N\N=C\C1=CC=CC=C1 JGOAZQAXRONCCI-SDNWHVSQSA-N 0.000 abstract 1
- 230000003647 oxidation Effects 0.000 abstract 1
- 238000007254 oxidation reaction Methods 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- SRRKNRDXURUMPP-UHFFFAOYSA-N sodium disulfide Chemical compound [Na+].[Na+].[S-][S-] SRRKNRDXURUMPP-UHFFFAOYSA-N 0.000 abstract 1
- 239000008107 starch Substances 0.000 abstract 1
- 235000019698 starch Nutrition 0.000 abstract 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 abstract 1
- 239000001117 sulphuric acid Substances 0.000 abstract 1
- 235000011149 sulphuric acid Nutrition 0.000 abstract 1
- 239000000454 talc Substances 0.000 abstract 1
- 229910052623 talc Inorganic materials 0.000 abstract 1
- 235000012222 talc Nutrition 0.000 abstract 1
- 235000015112 vegetable and seed oil Nutrition 0.000 abstract 1
- 239000008158 vegetable oil Substances 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pyridine Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEM55402A DE1193049B (de) | 1963-01-12 | 1963-01-12 | Verfahren zur Herstellung eines schwefelhaltigen Derivats des Vitamins B |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1005649A true GB1005649A (en) | 1965-09-22 |
Family
ID=7308294
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB866/64A Expired GB1005649A (en) | 1963-01-12 | 1964-01-08 | A sulphur-containing derivative of vitamin b and processes for its manufacture |
Country Status (9)
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3008963A (en) * | 1961-11-14 | Production of pyridine aldehydes | ||
| US2581869A (en) * | 1946-10-04 | 1952-01-08 | Monsanto Chemicals | N-(5-halo-2-thenyl)-substituted ethylene diamines |
| US2510893A (en) * | 1946-12-20 | 1950-06-06 | Velsicol Corp | Production of organo-thiyl compounds |
| US2510894A (en) * | 1946-12-20 | 1950-06-06 | Velsicol Corp | Production of organo-thiyl compounds |
| US2543544A (en) * | 1948-05-08 | 1951-02-27 | Indiana University Foundation | N, n-dimethyl-n'-(3-thienylmethyl)-n'-(alpha-pyridyl)-ethylenediamine |
| US3090726A (en) * | 1957-06-24 | 1963-05-21 | Carter Prod Inc | Novel composition of matter for treatment of nervous disorders |
| BE633927A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1958-03-21 | |||
| FR51M (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1960-06-03 | 1960-11-28 | ||
| US3067205A (en) * | 1960-10-12 | 1962-12-04 | United States Steel Corp | Method of making pyridine aldehydes |
-
0
- NL NL301345D patent/NL301345A/xx unknown
-
1963
- 1963-01-12 DE DEM55402A patent/DE1193049B/de active Pending
- 1963-10-25 CH CH1311863A patent/CH435276A/de unknown
- 1963-11-28 FI FI2344/63A patent/FI42329B/fi active
- 1963-12-04 NL NL63301345A patent/NL140522B/xx unknown
- 1963-12-13 FR FR957102A patent/FR3091M/fr active Active
- 1963-12-17 BR BR155478/63A patent/BR6355478D0/pt unknown
- 1963-12-26 US US333725A patent/US3296271A/en not_active Expired - Lifetime
-
1964
- 1964-01-06 DK DK4864AA patent/DK109446C/da active
- 1964-01-08 GB GB866/64A patent/GB1005649A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| CH435276A (de) | 1967-05-15 |
| US3296271A (en) | 1967-01-03 |
| BR6355478D0 (pt) | 1973-08-07 |
| FI42329B (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1970-03-31 |
| NL140522B (nl) | 1973-12-17 |
| DK109446C (da) | 1968-04-29 |
| FR3091M (fr) | 1965-01-25 |
| NL301345A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | |
| DE1193049B (de) | 1965-05-20 |
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