JPH0516424B2 - - Google Patents
Info
- Publication number
- JPH0516424B2 JPH0516424B2 JP59252083A JP25208384A JPH0516424B2 JP H0516424 B2 JPH0516424 B2 JP H0516424B2 JP 59252083 A JP59252083 A JP 59252083A JP 25208384 A JP25208384 A JP 25208384A JP H0516424 B2 JPH0516424 B2 JP H0516424B2
- Authority
- JP
- Japan
- Prior art keywords
- phenoxyethyl
- formula
- amide
- ethyl
- phosgene
- 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 - Lifetime
Links
- 238000000034 method Methods 0.000 claims description 26
- 150000001408 amides Chemical class 0.000 claims description 14
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical group ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 claims description 12
- -1 carbazate ester Chemical class 0.000 claims description 9
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical group ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 claims description 8
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 7
- 150000001875 compounds Chemical class 0.000 claims description 7
- LERXMGDFVFWGFQ-UHFFFAOYSA-N n-(2-phenoxyethyl)propanamide Chemical compound CCC(=O)NCCOC1=CC=CC=C1 LERXMGDFVFWGFQ-UHFFFAOYSA-N 0.000 claims description 7
- NYEZZYQZRQDLEH-UHFFFAOYSA-N 2-ethyl-4,5-dihydro-1,3-oxazole Chemical compound CCC1=NCCO1 NYEZZYQZRQDLEH-UHFFFAOYSA-N 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 6
- OWIUPIRUAQMTTK-UHFFFAOYSA-M n-aminocarbamate Chemical compound NNC([O-])=O OWIUPIRUAQMTTK-UHFFFAOYSA-M 0.000 claims description 6
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical group ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 claims description 6
- 239000012190 activator Substances 0.000 claims description 5
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical group COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 claims description 5
- 239000012458 free base Substances 0.000 claims description 5
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 5
- 238000010438 heat treatment Methods 0.000 claims description 4
- 238000010992 reflux Methods 0.000 claims description 4
- 238000000926 separation method Methods 0.000 claims description 4
- 239000002253 acid Substances 0.000 claims description 3
- 150000002148 esters Chemical class 0.000 claims description 3
- 150000002465 imidoyl halides Chemical class 0.000 claims description 3
- HFRXJVQOXRXOPP-UHFFFAOYSA-N thionyl bromide Chemical group BrS(Br)=O HFRXJVQOXRXOPP-UHFFFAOYSA-N 0.000 claims description 3
- OSFBJERFMQCEQY-UHFFFAOYSA-N propylidene Chemical group [CH]CC OSFBJERFMQCEQY-UHFFFAOYSA-N 0.000 claims description 2
- 150000003839 salts Chemical class 0.000 claims description 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 1
- 150000001450 anions Chemical class 0.000 claims 1
- 238000010924 continuous production Methods 0.000 claims 1
- 239000003960 organic solvent Substances 0.000 claims 1
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 24
- 239000000543 intermediate Substances 0.000 description 16
- 239000000047 product Substances 0.000 description 10
- 239000007787 solid Substances 0.000 description 10
- 238000006243 chemical reaction Methods 0.000 description 9
- 239000000203 mixture Substances 0.000 description 9
- 238000002844 melting Methods 0.000 description 8
- 230000008018 melting Effects 0.000 description 8
- 238000003756 stirring Methods 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 5
- WFJRIDQGVSJLLH-UHFFFAOYSA-N methyl n-aminocarbamate Chemical compound COC(=O)NN WFJRIDQGVSJLLH-UHFFFAOYSA-N 0.000 description 5
- FFSJPOPLSWBGQY-UHFFFAOYSA-N triazol-4-one Chemical compound O=C1C=NN=N1 FFSJPOPLSWBGQY-UHFFFAOYSA-N 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 238000005481 NMR spectroscopy Methods 0.000 description 4
- 230000004913 activation Effects 0.000 description 4
- 239000010410 layer Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- 239000003153 chemical reaction reagent Substances 0.000 description 3
- IXCSERBJSXMMFS-UHFFFAOYSA-N hcl hcl Chemical compound Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 150000002989 phenols Chemical class 0.000 description 3
- 238000001308 synthesis method Methods 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- JVLRNANYLVRULL-UHFFFAOYSA-N 1-(3-chlorophenyl)-4-(3-chloropropyl)piperazine;hydrochloride Chemical compound [Cl-].C1CN(CCCCl)CC[NH+]1C1=CC=CC(Cl)=C1 JVLRNANYLVRULL-UHFFFAOYSA-N 0.000 description 2
- IMSODMZESSGVBE-UHFFFAOYSA-N 2-Oxazoline Chemical compound C1CN=CO1 IMSODMZESSGVBE-UHFFFAOYSA-N 0.000 description 2
- STUGRPIYVZOYAH-UHFFFAOYSA-N 3-ethyl-4-(2-phenoxyethyl)-1h-1,2,4-triazol-5-one Chemical compound CCC1=NNC(=O)N1CCOC1=CC=CC=C1 STUGRPIYVZOYAH-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 208000020401 Depressive disease Diseases 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- 230000003213 activating effect Effects 0.000 description 2
- 150000001411 amidrazones Chemical class 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- VYSYZMNJHYOXGN-UHFFFAOYSA-N ethyl n-aminocarbamate Chemical compound CCOC(=O)NN VYSYZMNJHYOXGN-UHFFFAOYSA-N 0.000 description 2
- 239000002808 molecular sieve Substances 0.000 description 2
- VRBKIVRKKCLPHA-UHFFFAOYSA-N nefazodone Chemical compound O=C1N(CCOC=2C=CC=CC=2)C(CC)=NN1CCCN(CC1)CCN1C1=CC=CC(Cl)=C1 VRBKIVRKKCLPHA-UHFFFAOYSA-N 0.000 description 2
- 229960001800 nefazodone Drugs 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 2
- 230000003595 spectral effect Effects 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 238000005292 vacuum distillation Methods 0.000 description 2
- NWZSZGALRFJKBT-KNIFDHDWSA-N (2s)-2,6-diaminohexanoic acid;(2s)-2-hydroxybutanedioic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O.NCCCC[C@H](N)C(O)=O NWZSZGALRFJKBT-KNIFDHDWSA-N 0.000 description 1
- NSPMIYGKQJPBQR-UHFFFAOYSA-N 4H-1,2,4-triazole Chemical compound C=1N=CNN=1 NSPMIYGKQJPBQR-UHFFFAOYSA-N 0.000 description 1
- BHFXCANNBMNGPX-UHFFFAOYSA-N 5-(2-phenoxyethyl)-1,2,4-triazol-3-one Chemical compound O=C1N=NC(CCOC=2C=CC=CC=2)=N1 BHFXCANNBMNGPX-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- PTJGLFIIZFVFJV-UHFFFAOYSA-N N'-hydroxy-N-(3-pyridinyl)octanediamide Chemical compound ONC(=O)CCCCCCC(=O)NC1=CC=CN=C1 PTJGLFIIZFVFJV-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- QIOZLISABUUKJY-UHFFFAOYSA-N Thiobenzamide Chemical compound NC(=S)C1=CC=CC=C1 QIOZLISABUUKJY-UHFFFAOYSA-N 0.000 description 1
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000002610 basifying agent Substances 0.000 description 1
- FFBHFFJDDLITSX-UHFFFAOYSA-N benzyl N-[2-hydroxy-4-(3-oxomorpholin-4-yl)phenyl]carbamate Chemical compound OC1=C(NC(=O)OCC2=CC=CC=C2)C=CC(=C1)N1CCOCC1=O FFBHFFJDDLITSX-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 244000309464 bull Species 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- IEJIGPNLZYLLBP-UHFFFAOYSA-N dimethyl carbonate Chemical compound COC(=O)OC IEJIGPNLZYLLBP-UHFFFAOYSA-N 0.000 description 1
- 238000000921 elemental analysis Methods 0.000 description 1
- AEOCXXJPGCBFJA-UHFFFAOYSA-N ethionamide Chemical compound CCC1=CC(C(N)=S)=CC=N1 AEOCXXJPGCBFJA-UHFFFAOYSA-N 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- IKDUDTNKRLTJSI-UHFFFAOYSA-N hydrazine monohydrate Substances O.NN IKDUDTNKRLTJSI-UHFFFAOYSA-N 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 150000002466 imines Chemical group 0.000 description 1
- 239000013067 intermediate product Substances 0.000 description 1
- 238000011031 large-scale manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 239000012044 organic layer Substances 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- RLOWWWKZYUNIDI-UHFFFAOYSA-N phosphinic chloride Chemical compound ClP=O RLOWWWKZYUNIDI-UHFFFAOYSA-N 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 150000003140 primary amides Chemical class 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 150000003334 secondary amides Chemical class 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
- CZDYPVPMEAXLPK-UHFFFAOYSA-N tetramethylsilane Chemical compound C[Si](C)(C)C CZDYPVPMEAXLPK-UHFFFAOYSA-N 0.000 description 1
- 150000003556 thioamides Chemical class 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
- C07D249/10—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D249/12—Oxygen or sulfur atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Coloring (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US55672783A | 1983-11-30 | 1983-11-30 | |
| US556727 | 1983-11-30 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS60132969A JPS60132969A (ja) | 1985-07-16 |
| JPH0516424B2 true JPH0516424B2 (nl) | 1993-03-04 |
Family
ID=24222593
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP59252083A Granted JPS60132969A (ja) | 1983-11-30 | 1984-11-30 | ４‐（２‐フエノキシエチル）‐１，２，４‐トリアゾロン製法 |
Country Status (25)
| Country | Link |
|---|---|
| JP (1) | JPS60132969A (nl) |
| KR (1) | KR890000990B1 (nl) |
| AT (1) | AT387571B (nl) |
| AU (1) | AU576338B2 (nl) |
| BE (1) | BE901165A (nl) |
| CA (1) | CA1233826A (nl) |
| CH (1) | CH663613A5 (nl) |
| CY (2) | CY1472A (nl) |
| DE (1) | DE3443820C2 (nl) |
| DK (3) | DK159970C (nl) |
| ES (2) | ES8609282A1 (nl) |
| FI (1) | FI81785C (nl) |
| FR (1) | FR2555582B1 (nl) |
| GB (2) | GB2150567B (nl) |
| GR (1) | GR81110B (nl) |
| HK (2) | HK16289A (nl) |
| IE (1) | IE74871B1 (nl) |
| IT (1) | IT1178641B (nl) |
| KE (1) | KE3852A (nl) |
| LU (1) | LU85657A1 (nl) |
| NL (1) | NL8403635A (nl) |
| SE (3) | SE456993B (nl) |
| SG (1) | SG80588G (nl) |
| YU (2) | YU44721B (nl) |
| ZA (1) | ZA849264B (nl) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2182241C (en) * | 1996-07-29 | 2002-09-17 | Bo Lei | Methods for the manufacture of nefazodone |
| DE19902960A1 (de) * | 1999-01-26 | 2000-07-27 | Bayer Ag | Verfahren zur Herstellung von Methylcarbazat |
| CA2356450C (en) | 2001-09-10 | 2003-11-25 | Brantford Chemicals Inc. | An improved process for the preparation of nefazodone hydrochloride |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1126882B (de) * | 1960-05-03 | 1962-04-05 | Boehringer Sohn Ingelheim | Verfahren zur Herstellung von 1,2,4-Triazolonen-(5) |
| DE1545646B1 (de) * | 1965-12-15 | 1969-09-18 | Boehringer Sohn Ingelheim | 1,3-Dimethyl-4-(2',4'-dichlorphenyl)-1,2,4-triazolon-(5) und Verfahren zu dessen Herstellung |
| US4338317A (en) * | 1981-03-16 | 1982-07-06 | Mead Johnson & Company | Phenoxyethyl-1,2,4,-triazol-3-one antidepressants |
| US4487773A (en) * | 1981-03-16 | 1984-12-11 | Mead Johnson & Company | 1,2,4-Triazol-3-one antidepressants |
| US4613600A (en) * | 1983-09-30 | 1986-09-23 | Mead Johnson & Company | Antidepressant 1,2,4-triazolone compounds |
-
1984
- 1984-11-26 YU YU1998/84A patent/YU44721B/xx unknown
- 1984-11-27 ZA ZA849264A patent/ZA849264B/xx unknown
- 1984-11-27 FI FI844647A patent/FI81785C/fi active IP Right Grant
- 1984-11-29 SE SE8406045A patent/SE456993B/sv not_active IP Right Cessation
- 1984-11-29 IE IE305984A patent/IE74871B1/en not_active IP Right Cessation
- 1984-11-29 ES ES538079A patent/ES8609282A1/es not_active Expired
- 1984-11-29 CH CH5700/84A patent/CH663613A5/de not_active IP Right Cessation
- 1984-11-29 FR FR8418173A patent/FR2555582B1/fr not_active Expired
- 1984-11-29 BE BE0/214083A patent/BE901165A/fr not_active IP Right Cessation
- 1984-11-29 NL NL8403635A patent/NL8403635A/nl active Search and Examination
- 1984-11-29 GR GR81110A patent/GR81110B/el unknown
- 1984-11-29 DK DK567384A patent/DK159970C/da not_active IP Right Cessation
- 1984-11-29 CA CA000468894A patent/CA1233826A/en not_active Expired
- 1984-11-29 IT IT23808/84A patent/IT1178641B/it active
- 1984-11-29 LU LU85657A patent/LU85657A1/xx unknown
- 1984-11-30 JP JP59252083A patent/JPS60132969A/ja active Granted
- 1984-11-30 AT AT0380884A patent/AT387571B/de not_active IP Right Cessation
- 1984-11-30 DE DE3443820A patent/DE3443820C2/de not_active Expired - Lifetime
- 1984-11-30 KR KR1019840007553A patent/KR890000990B1/ko not_active IP Right Cessation
- 1984-11-30 GB GB08430275A patent/GB2150567B/en not_active Expired
- 1984-11-30 AU AU36092/84A patent/AU576338B2/en not_active Expired
-
1986
- 1986-03-31 ES ES553547A patent/ES8706320A1/es not_active Expired
- 1986-05-20 YU YU826/86A patent/YU45325B/xx unknown
-
1987
- 1987-02-02 GB GB08702275A patent/GB2185983B/en not_active Expired
-
1988
- 1988-04-15 SE SE8801409A patent/SE469894B/sv not_active IP Right Cessation
- 1988-04-15 SE SE8801408A patent/SE464025B/sv not_active IP Right Cessation
- 1988-11-30 SG SG805/88A patent/SG80588G/en unknown
- 1988-12-21 KE KE3852A patent/KE3852A/xx unknown
-
1989
- 1989-02-23 HK HK162/89A patent/HK16289A/xx not_active IP Right Cessation
- 1989-02-23 HK HK163/89A patent/HK16389A/xx not_active IP Right Cessation
- 1989-07-21 CY CY1472A patent/CY1472A/xx unknown
- 1989-07-21 CY CY1471A patent/CY1471A/xx unknown
-
1990
- 1990-03-19 DK DK070890A patent/DK70890A/da not_active Application Discontinuation
- 1990-03-19 DK DK070790A patent/DK171451B1/da not_active IP Right Cessation
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| WO2010031497A1 (en) | New process for the preparation of iloperidone | |
| JPH0516424B2 (nl) | ||
| US4596884A (en) | 4-(2-phenoxyethyl)-1,2,4-triazolone process intermediates | |
| WO2001085657A1 (en) | Synthesis of cyclohexene dimethanol compounds | |
| US10640467B2 (en) | Process for preparing 2-(1-(tert-butoxycarbonyl)piperidine-4-yl)benzoic acid | |
| SK20192000A3 (sk) | Soli n-terc-butylhydroxylamínu | |
| JPS588065A (ja) | エタンブト−ルスルホン酸誘導体の製造方法 | |
| KR101811123B1 (ko) | 신규의 모르폴린 이인산염 및 이를 이용한 고순도 리바록사반의 제조방법 | |
| US6248888B1 (en) | Process for the preparation of terazosin hydrochloride dihydrate | |
| US4071684A (en) | Process for producing 3-substituted 1,2,4-triazines | |
| WO1992004329A1 (en) | Process for producing nitrogenous heterocycle | |
| CA2356450C (en) | An improved process for the preparation of nefazodone hydrochloride | |
| JPH09124605A (ja) | ３，４−ジヒドロカルボスチリルの製造方法 | |
| FI83637B (fi) | Syraadditionssalter av alkyl-1-/ (2-fenoxietyl)amino/propylidenhydrazinkarboxylat och foerfarande foer deras framstaellning. | |
| JPS6038364A (ja) | エチレン尿素及びその製造方法 | |
| JP4305747B2 (ja) | ２−フェニル−４−（ジクロロフェニル）イミダゾール化合物 | |
| CA1085846A (en) | Process for producing 3-substituted 1,2,4-triazines | |
| JPH0827148A (ja) | ジチアゾリウム塩の製造方法 | |
| JP2554603B2 (ja) | 光学活性４−（２−メチルプロピル）−５−フエニル−１，３−オキサゾリジン−２−オンの製法 | |
| IE63909B1 (en) | Intermediates in process for production of 1,2,4-triazolones | |
| JPH0481989B2 (nl) | ||
| JPH0133104B2 (nl) | ||
| JPH0344065B2 (nl) | ||
| JPH0524906B2 (nl) | ||
| JPH1180062A (ja) | ビス｛β−（ｐ−メトキシフェノキシ）エチル｝エーテルの製造方法 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| EXPY | Cancellation because of completion of term |