GB1433013A - - Google Patents
Info
- Publication number
- GB1433013A GB1433013A GB2747173A GB2747173A GB1433013A GB 1433013 A GB1433013 A GB 1433013A GB 2747173 A GB2747173 A GB 2747173A GB 2747173 A GB2747173 A GB 2747173A GB 1433013 A GB1433013 A GB 1433013A
- Authority
- GB
- United Kingdom
- Prior art keywords
- diphenyl
- alkyl
- formula
- trans
- substituted
- 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
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/04—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
- C07D311/58—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring other than with oxygen or sulphur atoms in position 2 or 4
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
1433013 Substituted trans - 3,4 - (diphenyl)- chromans RIKER LABORATORIES Inc 8 June 1973 27471/73 Heading C2C A process for the production of a substituted trans-3,4-(diphenyl)-chroman of the formula wherein R is (C 1 -C 6 ) alkyl; R<SP>3</SP> is (C 1 -C 6 ) alkyl or alkoxy, halogen or trifluoromethyl; Alk is (C 2 -C 6 ) alkylene; R<SP>1</SP> and R<SP>3</SP> are hydrogen or (C 1 -C 6 ) alkyl or, together with the nitrogen atom to which they are attached, form a pyrrolidino morpholino, piperidino, piperazino, 4-alkylpiperazino or 4-phenylpiperazino radical, comprises catalytically rearranging the corresponding cis compound by treatment with an organo-lithium or alkali metal alkoxide catalyst. The cis isomer is suitably prepared by catalytically hydrogenating a substituted 3,4-(diphenyl) chromene of the formula and reacting the chroman so formed with a compound of the formula: X.Alk.NR<SP>1</SP>R<SP>2</SP>, wherein X is halogen. The process is also suitable for converting a cis, trans isomer mixture into the trans isomer.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2747173A GB1433013A (en) | 1973-06-08 | 1973-06-08 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2747173A GB1433013A (en) | 1973-06-08 | 1973-06-08 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1433013A true GB1433013A (en) | 1976-04-22 |
Family
ID=10260138
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2747173A Expired GB1433013A (en) | 1973-06-08 | 1973-06-08 |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB1433013A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7601855B2 (en) | 2004-09-21 | 2009-10-13 | Novogen Research Pty Ltd | Substituted chroman derivatives, medicaments and use in therapy |
US8080675B2 (en) | 2004-09-21 | 2011-12-20 | Marshall Edwards, Inc. | Chroman derivatives, medicaments and use in therapy |
US9663484B2 (en) | 2010-11-01 | 2017-05-30 | Mei Pharma, Inc. | Isoflavonoid compounds and methods for the treatment of cancer |
US10980774B2 (en) | 2015-02-02 | 2021-04-20 | Mei Pharma, Inc. | Combination therapies |
-
1973
- 1973-06-08 GB GB2747173A patent/GB1433013A/en not_active Expired
Cited By (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9381186B2 (en) | 2004-09-21 | 2016-07-05 | Mei Pharma, Inc. | Substituted chroman derivatives, medicaments and use in therapy |
US8084628B2 (en) | 2004-09-21 | 2011-12-27 | Marshall Edwards, Inc. | Substituted chroman derivatives, medicaments and use in therapy |
US7601855B2 (en) | 2004-09-21 | 2009-10-13 | Novogen Research Pty Ltd | Substituted chroman derivatives, medicaments and use in therapy |
US8461361B2 (en) | 2004-09-21 | 2013-06-11 | Marshall Edwards, Inc. | Chroman derivatives, medicaments and use in therapy |
US8697891B2 (en) | 2004-09-21 | 2014-04-15 | Marshall Edwards, Inc. | Substituted chroman derivatives, medicaments and use in therapy |
US8957109B2 (en) | 2004-09-21 | 2015-02-17 | Mei Pharma, Inc. | Chroman derivatives, medicaments and use in therapy |
US9138478B2 (en) | 2004-09-21 | 2015-09-22 | Mei Pharma, Inc. | Substituted chroman derivatives, medicaments and use in therapy |
US9198895B2 (en) | 2004-09-21 | 2015-12-01 | Mei Pharma, Inc. | Chroman derivatives, medicaments and use in therapy |
US8080675B2 (en) | 2004-09-21 | 2011-12-20 | Marshall Edwards, Inc. | Chroman derivatives, medicaments and use in therapy |
US11723893B2 (en) | 2010-11-01 | 2023-08-15 | Mei Pharma, Inc. | Isoflavonoid compositions and methods for the treatment of cancer |
US9708283B2 (en) | 2010-11-01 | 2017-07-18 | Mei Pharma, Inc. | Isoflavonoid compositions and methods for the treatment of cancer |
US9981936B2 (en) | 2010-11-01 | 2018-05-29 | Mei Pharma, Inc. | Isoflavonoid compositions and methods for the treatment of cancer |
US10105346B2 (en) | 2010-11-01 | 2018-10-23 | Mei Pharma, Inc. | Isoflavonoid compounds and methods for the treatment of cancer |
US10369132B2 (en) | 2010-11-01 | 2019-08-06 | Mei Pharma, Inc. | Isoflavonoid compositions and methods for the treatment of cancer |
US10973799B2 (en) | 2010-11-01 | 2021-04-13 | Mei Pharma, Inc. | Isoflavonoid compositions and methods for the treatment of cancer |
US11583514B2 (en) | 2010-11-01 | 2023-02-21 | Mei Pharma, Inc. | Isoflavonoid compounds and methods for the treatment of cancer |
US9663484B2 (en) | 2010-11-01 | 2017-05-30 | Mei Pharma, Inc. | Isoflavonoid compounds and methods for the treatment of cancer |
US10980774B2 (en) | 2015-02-02 | 2021-04-20 | Mei Pharma, Inc. | Combination therapies |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PCNP | Patent ceased through non-payment of renewal fee |