BE831390A - Procede de preparation du fumarate acide de la 3-(1-benzylcycloheptyl)oxy-n,n-dimethylpropylamine - Google Patents
Procede de preparation du fumarate acide de la 3-(1-benzylcycloheptyl)oxy-n,n-dimethylpropylamineInfo
- Publication number
- BE831390A BE831390A BE158318A BE158318A BE831390A BE 831390 A BE831390 A BE 831390A BE 158318 A BE158318 A BE 158318A BE 158318 A BE158318 A BE 158318A BE 831390 A BE831390 A BE 831390A
- Authority
- BE
- Belgium
- Prior art keywords
- dimethylpropylamine
- formula
- emi
- oxy
- preparation
- Prior art date
Links
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 title claims description 6
- 239000002253 acid Substances 0.000 title claims description 3
- FYJJXENSONZJRG-UHFFFAOYSA-N bencyclane Chemical compound C=1C=CC=CC=1CC1(OCCCN(C)C)CCCCCC1 FYJJXENSONZJRG-UHFFFAOYSA-N 0.000 title claims description 3
- 238000000034 method Methods 0.000 title description 4
- 238000002360 preparation method Methods 0.000 title description 4
- VZCYOOQTPOCHFL-OWOJBTEDSA-L fumarate(2-) Chemical compound [O-]C(=O)\C=C\C([O-])=O VZCYOOQTPOCHFL-OWOJBTEDSA-L 0.000 title 1
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 claims description 8
- RTRTUCOUELDWEX-UHFFFAOYSA-N 1-benzylcycloheptan-1-ol Chemical compound C=1C=CC=CC=1CC1(O)CCCCCC1 RTRTUCOUELDWEX-UHFFFAOYSA-N 0.000 claims description 4
- JLIDRDJNLAWIKT-UHFFFAOYSA-N 1,2-dimethyl-3h-benzo[e]indole Chemical compound C1=CC=CC2=C(C(=C(C)N3)C)C3=CC=C21 JLIDRDJNLAWIKT-UHFFFAOYSA-N 0.000 claims description 3
- NYYRRBOMNHUCLB-UHFFFAOYSA-N 3-chloro-n,n-dimethylpropan-1-amine Chemical compound CN(C)CCCCl NYYRRBOMNHUCLB-UHFFFAOYSA-N 0.000 claims description 3
- DULCUDSUACXJJC-UHFFFAOYSA-N benzeneacetic acid ethyl ester Natural products CCOC(=O)CC1=CC=CC=C1 DULCUDSUACXJJC-UHFFFAOYSA-N 0.000 claims description 3
- 239000001530 fumaric acid Substances 0.000 claims description 3
- ODZPKZBBUMBTMG-UHFFFAOYSA-N sodium amide Chemical compound [NH2-].[Na+] ODZPKZBBUMBTMG-UHFFFAOYSA-N 0.000 claims description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
- 239000000460 chlorine Substances 0.000 claims description 2
- 229910052801 chlorine Inorganic materials 0.000 claims description 2
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 12
- 239000000203 mixture Substances 0.000 description 10
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- SGRHVVLXEBNBDV-UHFFFAOYSA-N 1,6-dibromohexane Chemical compound BrCCCCCCBr SGRHVVLXEBNBDV-UHFFFAOYSA-N 0.000 description 1
- -1 1-benzylcycloheptyl Chemical group 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- CGZZMOTZOONQIA-UHFFFAOYSA-N cycloheptanone Chemical compound O=C1CCCCCC1 CGZZMOTZOONQIA-UHFFFAOYSA-N 0.000 description 1
- 125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000002329 infrared spectrum Methods 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT2622874A IT1064069B (it) | 1974-08-09 | 1974-08-09 | Processo per la preparazione del fumarato acido della 3 i benzil cicloeptil ossi n.n dimetil propilammina |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE831390A true BE831390A (fr) | 1975-11-03 |
Family
ID=11218995
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE158318A BE831390A (fr) | 1974-08-09 | 1975-07-15 | Procede de preparation du fumarate acide de la 3-(1-benzylcycloheptyl)oxy-n,n-dimethylpropylamine |
Country Status (6)
| Country | Link |
|---|---|
| BE (1) | BE831390A (es) |
| CH (1) | CH594599A5 (es) |
| ES (1) | ES440093A1 (es) |
| IT (1) | IT1064069B (es) |
| LU (1) | LU73171A1 (es) |
| NL (1) | NL7509288A (es) |
-
1974
- 1974-08-09 IT IT2622874A patent/IT1064069B/it active
-
1975
- 1975-07-15 BE BE158318A patent/BE831390A/fr unknown
- 1975-07-25 CH CH976475A patent/CH594599A5/xx not_active IP Right Cessation
- 1975-08-04 NL NL7509288A patent/NL7509288A/xx not_active Application Discontinuation
- 1975-08-07 LU LU73171A patent/LU73171A1/xx unknown
- 1975-08-08 ES ES440093A patent/ES440093A1/es not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| ES440093A1 (es) | 1977-02-16 |
| LU73171A1 (es) | 1976-03-02 |
| CH594599A5 (en) | 1978-01-13 |
| NL7509288A (nl) | 1976-02-11 |
| IT1064069B (it) | 1985-02-18 |
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