GB1034486A - Dibenzocycloheptene derivatives and their preparation - Google Patents
Dibenzocycloheptene derivatives and their preparationInfo
- Publication number
- GB1034486A GB1034486A GB20214/63A GB2021463A GB1034486A GB 1034486 A GB1034486 A GB 1034486A GB 20214/63 A GB20214/63 A GB 20214/63A GB 2021463 A GB2021463 A GB 2021463A GB 1034486 A GB1034486 A GB 1034486A
- Authority
- GB
- United Kingdom
- Prior art keywords
- dibenzo
- alkyl
- cycloheptene
- prepared
- dihydrocycloheptene
- 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
- 238000002360 preparation method Methods 0.000 title abstract 3
- 150000008508 dibenzocycloheptenes Chemical class 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 8
- -1 C1- 4 haloacylamino Chemical group 0.000 abstract 7
- 125000005843 halogen group Chemical group 0.000 abstract 5
- 239000004215 Carbon black (E152) Substances 0.000 abstract 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 229930195733 hydrocarbon Natural products 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 230000003301 hydrolyzing effect Effects 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- UHZYTMXLRWXGPK-UHFFFAOYSA-N phosphorus pentachloride Chemical compound ClP(Cl)(Cl)(Cl)Cl UHZYTMXLRWXGPK-UHFFFAOYSA-N 0.000 abstract 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 2
- 125000006561 (C1-C5) alkylsulphonylamino group Chemical group 0.000 abstract 1
- XUDMFUCJNFYMRZ-UHFFFAOYSA-N 11-chloro-11h-dibenzo[1,2-a:1',2'-e][7]annulene Chemical compound C1=CC2=CC=CC=C2C(Cl)C2=CC=CC=C21 XUDMFUCJNFYMRZ-UHFFFAOYSA-N 0.000 abstract 1
- MKKZZGYCTNAUEU-UHFFFAOYSA-N 11-cyclopropyldibenzo[1,2-a:1',2'-e][7]annulen-11-ol Chemical compound C12=CC=CC=C2C=CC2=CC=CC=C2C1(O)C1CC1 MKKZZGYCTNAUEU-UHFFFAOYSA-N 0.000 abstract 1
- BAIZMUSHFGWYFC-UHFFFAOYSA-N 5-chlorodibenzo[1,2-a:1',2'-e][7]annulen-11-one Chemical compound ClC1=CC2=CC=CC=C2C(=O)C2=CC=CC=C12 BAIZMUSHFGWYFC-UHFFFAOYSA-N 0.000 abstract 1
- LGZTUCWBCXRRNZ-UHFFFAOYSA-N 9-chloro-2-cyclopropyltricyclo[9.4.0.03,8]pentadeca-1(15),3,5,7,9,11,13-heptaen-2-ol Chemical compound C1(CC1)C1(C2=C(C(=CC3=C1C=CC=C3)Cl)C=CC=C2)O LGZTUCWBCXRRNZ-UHFFFAOYSA-N 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical group O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 abstract 1
- 125000002252 acyl group Chemical group 0.000 abstract 1
- 125000004442 acylamino group Chemical group 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000003282 alkyl amino group Chemical group 0.000 abstract 1
- 125000002877 alkyl aryl group Chemical group 0.000 abstract 1
- 125000005115 alkyl carbamoyl group Chemical group 0.000 abstract 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 1
- 125000004414 alkyl thio group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- QPJORFLSOJAUNL-UHFFFAOYSA-N dibenzo[a,d][7]annulene Chemical class C1=CC2=CC=CC=C2CC2=CC=CC=C21 QPJORFLSOJAUNL-UHFFFAOYSA-N 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 150000004820 halides Chemical class 0.000 abstract 1
- 125000005252 haloacyl group Chemical group 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- VFZXMEQGIIWBFJ-UHFFFAOYSA-M magnesium;cyclopropane;bromide Chemical compound [Mg+2].[Br-].C1C[CH-]1 VFZXMEQGIIWBFJ-UHFFFAOYSA-M 0.000 abstract 1
- DQEUYIQDSMINEY-UHFFFAOYSA-M magnesium;prop-1-ene;bromide Chemical compound [Mg+2].[Br-].[CH2-]C=C DQEUYIQDSMINEY-UHFFFAOYSA-M 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 125000003396 thiol group Chemical class [H]S* 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
- C07C309/63—Esters of sulfonic acids
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US20065962A | 1962-06-07 | 1962-06-07 | |
| US470228A US3332977A (en) | 1962-06-07 | 1965-07-07 | 5-(gamma-hydrocarbonyl-sulfonyloxypropyl-and gamma-hydrocarbamyl-sulfonyl-oxypropylidene)-5h-dibenzo[a, d]-cycloheptene compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1034486A true GB1034486A (en) | 1966-06-29 |
Family
ID=26895969
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB20214/63A Expired GB1034486A (en) | 1962-06-07 | 1963-05-21 | Dibenzocycloheptene derivatives and their preparation |
Country Status (7)
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7446227B2 (en) * | 2006-12-11 | 2008-11-04 | Apicore, Llc | Process for preparation of 5H-dibenzo[a,d] cycloheptene derivatives |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1543035A1 (de) * | 1965-01-06 | 1969-09-25 | Hoffmann La Roche | Verfahren zur Herstellung von Dibenzocycloheptenverbindungen |
| US3478048A (en) * | 1965-01-08 | 1969-11-11 | Hoffmann La Roche | 2,3;3a,12b - tetrahydro - 8h - dibenzo (3,4;6,7)cyclohept(1,2-d)oxazoles and derivatives |
| CH471772A (de) * | 1966-03-17 | 1969-04-30 | Hoffmann La Roche | Verfahren zur Herstellung von tricyclischen Aminen |
| SE354866B (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1968-10-09 | 1973-03-26 | Leo Ab |
-
0
- NL NL293802D patent/NL293802A/xx unknown
-
1963
- 1963-05-21 GB GB20214/63A patent/GB1034486A/en not_active Expired
- 1963-05-31 DK DK260863AA patent/DK113916B/da unknown
- 1963-06-05 CH CH700363A patent/CH456577A/de unknown
- 1963-06-06 FI FI1158/63A patent/FI41021B/fi active
- 1963-06-06 SE SE6261/63A patent/SE318270B/xx unknown
-
1964
- 1964-03-23 DK DK147064AA patent/DK111818B/da unknown
-
1965
- 1965-07-07 US US470228A patent/US3332977A/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7446227B2 (en) * | 2006-12-11 | 2008-11-04 | Apicore, Llc | Process for preparation of 5H-dibenzo[a,d] cycloheptene derivatives |
Also Published As
| Publication number | Publication date |
|---|---|
| SE318270B (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1969-12-08 |
| DK113916B (da) | 1969-05-12 |
| FI41021B (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1969-04-30 |
| DK111818B (da) | 1968-10-14 |
| NL293802A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | |
| CH456577A (de) | 1968-07-31 |
| US3332977A (en) | 1967-07-25 |
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