SU1176833A3 - Способ получени производных фенилового эфира карбаминовой кислоты - Google Patents
Способ получени производных фенилового эфира карбаминовой кислоты Download PDFInfo
- Publication number
- SU1176833A3 SU1176833A3 SU803003801A SU3003801A SU1176833A3 SU 1176833 A3 SU1176833 A3 SU 1176833A3 SU 803003801 A SU803003801 A SU 803003801A SU 3003801 A SU3003801 A SU 3003801A SU 1176833 A3 SU1176833 A3 SU 1176833A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- general formula
- lower alkyl
- derivatives
- phenyl ether
- acid
- Prior art date
Links
- 239000002253 acid Substances 0.000 title claims abstract description 4
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical class C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 title abstract 2
- 238000000034 method Methods 0.000 title description 3
- CVXBEEMKQHEXEN-UHFFFAOYSA-N carbaryl Chemical compound C1=CC=C2C(OC(=O)NC)=CC=CC2=C1 CVXBEEMKQHEXEN-UHFFFAOYSA-N 0.000 title 1
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 claims abstract description 9
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 9
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims abstract description 3
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical group C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims abstract description 3
- 229910052801 chlorine Inorganic materials 0.000 claims abstract description 3
- 239000000460 chlorine Substances 0.000 claims abstract description 3
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims abstract description 3
- 125000006627 ethoxycarbonylamino group Chemical group 0.000 claims abstract description 3
- -1 sulfamide carbamoyl benzoic acid Chemical compound 0.000 claims abstract description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 3
- 230000010933 acylation Effects 0.000 claims abstract 3
- 238000005917 acylation reaction Methods 0.000 claims abstract 3
- 125000003545 alkoxy group Chemical group 0.000 claims abstract 2
- 238000004519 manufacturing process Methods 0.000 claims abstract 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims abstract 2
- 239000003960 organic solvent Substances 0.000 claims abstract 2
- 150000002989 phenols Chemical class 0.000 claims abstract 2
- HUMLZQGETGYMKU-UHFFFAOYSA-N carbamic acid;phenoxybenzene Chemical class NC(O)=O.C=1C=CC=CC=1OC1=CC=CC=C1 HUMLZQGETGYMKU-UHFFFAOYSA-N 0.000 claims 1
- 150000007529 inorganic bases Chemical class 0.000 claims 1
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 2
- KADIXIAYGVXKDW-UHFFFAOYSA-N (2-aminophenyl)-phenylcarbamic acid Chemical compound NC1=CC=CC=C1N(C(O)=O)C1=CC=CC=C1 KADIXIAYGVXKDW-UHFFFAOYSA-N 0.000 description 1
- SNBWUWQHPDWGKN-UHFFFAOYSA-N 3,3-diethylpentan-2-one Chemical compound CCC(CC)(CC)C(C)=O SNBWUWQHPDWGKN-UHFFFAOYSA-N 0.000 description 1
- 150000004703 alkoxides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-N carbonic acid monoamide Natural products NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 1
- 230000002363 herbicidal effect Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- FFQQCJGNKKIRMD-UHFFFAOYSA-N methyl n-(3-hydroxyphenyl)carbamate Chemical compound COC(=O)NC1=CC=CC(O)=C1 FFQQCJGNKKIRMD-UHFFFAOYSA-N 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- KJAMZCVTJDTESW-UHFFFAOYSA-N tiracizine Chemical compound C1CC2=CC=CC=C2N(C(=O)CN(C)C)C2=CC(NC(=O)OCC)=CC=C21 KJAMZCVTJDTESW-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/78—Benzo [b] furans; Hydrogenated benzo [b] furans
- C07D307/86—Benzo [b] furans; Hydrogenated benzo [b] furans with an oxygen atom directly attached in position 7
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
HUCI001984 HU184063B (en) | 1979-11-08 | 1979-11-08 | Process for producing carbamoic-acid-phenyl-ester derivatives |
Publications (1)
Publication Number | Publication Date |
---|---|
SU1176833A3 true SU1176833A3 (ru) | 1985-08-30 |
Family
ID=10994773
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SU803003801A SU1176833A3 (ru) | 1979-11-08 | 1980-11-05 | Способ получени производных фенилового эфира карбаминовой кислоты |
Country Status (10)
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
HU185294B (en) * | 1980-12-29 | 1984-12-28 | Chinoin Gyogyszer Es Vegyeszet | Process for producing substituted urea derivatives |
FR2612186B1 (fr) * | 1987-03-09 | 1989-07-21 | Poudres & Explosifs Ste Nale | Carbonyl 2,2' bis (alkyl-4 oxadiazolidines-1,2,4-diones-3,5), leur procede de preparation et leur utilisation comme intermediaires de synthese dans la preparation de carbamates |
DE3884070T2 (de) * | 1987-06-25 | 1994-01-13 | Dowelanco | Verfahren zur Herstellung von Harnstoffen. |
JP4821680B2 (ja) * | 2007-03-30 | 2011-11-24 | 大日本印刷株式会社 | 塩基増殖剤、それを用いた樹脂組成物、及び物品 |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE792313A (fr) * | 1971-12-06 | 1973-03-30 | Quimco Gmbh | Procede de preparation de carbamates mono substitues sur l'atome d'azote et produits obtenus |
HU167249B (enrdf_load_stackoverflow) * | 1973-04-24 | 1975-09-27 |
-
1979
- 1979-11-08 HU HUCI001984 patent/HU184063B/hu unknown
-
1980
- 1980-10-29 DE DE19803040633 patent/DE3040633A1/de active Granted
- 1980-11-04 YU YU280880A patent/YU280880A/xx unknown
- 1980-11-04 PL PL22765180A patent/PL127976B1/pl unknown
- 1980-11-04 CS CS744780A patent/CS219932B2/cs unknown
- 1980-11-05 FR FR8023596A patent/FR2469399A1/fr active Granted
- 1980-11-05 DD DD22498880A patent/DD154100A5/de not_active IP Right Cessation
- 1980-11-05 DD DD23091580A patent/DD159637A5/de not_active IP Right Cessation
- 1980-11-05 JP JP15476980A patent/JPS5683461A/ja active Pending
- 1980-11-05 SU SU803003801A patent/SU1176833A3/ru active
- 1980-11-06 GB GB8035667A patent/GB2065639B/en not_active Expired
Non-Patent Citations (1)
Title |
---|
Патент US № 4278807, кл. с 07 С 125/067, опублик.1981. Патент Венгрии № 154047, кл. 12011-18, опублик.1974; * |
Also Published As
Publication number | Publication date |
---|---|
DE3040633A1 (de) | 1981-05-21 |
YU280880A (en) | 1983-12-31 |
FR2469399B1 (enrdf_load_stackoverflow) | 1984-05-11 |
FR2469399A1 (fr) | 1981-05-22 |
DD154100A5 (de) | 1982-02-24 |
PL127976B1 (en) | 1983-12-31 |
CS219932B2 (en) | 1983-03-25 |
GB2065639B (en) | 1983-10-26 |
JPS5683461A (en) | 1981-07-08 |
DE3040633C2 (enrdf_load_stackoverflow) | 1989-01-05 |
HU184063B (en) | 1984-06-28 |
GB2065639A (en) | 1981-07-01 |
DD159637A5 (de) | 1983-03-23 |
PL227651A1 (enrdf_load_stackoverflow) | 1981-08-21 |
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