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Process for the preparation of carbamate derivatives

Assignee: Chinoin Private Co Ltd
•
Filing: 1976-04-30
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Granted: 1978-04-25
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Expires: 1996-04-30
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Abstract

Abstract A process for the preparation of a compound of the formula: ##STR1## wherein R 1 is alkyl, alkyl substituted by halogen, alkyl substituted by alkoxy, aryl, aryl substituted by halogen, aryl substituted by alkyl, aryl substituted by alkoxy, aralkyl, aralkyl substituted by alkoxy, cycloalkyl, cycloalkyl substituted by halogen, cycloalkyl substituted by alkyl or cycloalkyl substituted by alkoxy, and R 2 is an aromatic group, an aromatic group substituted by alkyl, an aromatic group substituted by halogen, an aromatic group substituted by alkoxy, a heteroaromatic group, a heteroaromatic group substituted by alkyl, a heteroaromatic group substituted by halogen, or a heteroaromatic group substituted by alkoxy, by the reaction of phosgene with a phenol of the formula: R.sup.2 -OH and further by the reaction of a primary amine of the formula: R'--NH.sub.2, reacting all three of the abovementioned reactants solution in a common water-immiscible organic solvent in the same reaction vessel at the same time in the presence of an acid binding agent to yield the compound of formula ##STR2##

Inventors

  • 👤 Geza Toth
  • 👤 Istvan Toth
  • 👤 Tibor Montay

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-30 22:47
CPC Classifications
C; C07; C07D; C07D235/00; C07D235/02; C07D235/04; C07D235/24; C07D235/30; C07D235/32; C07C; C07C273/00; C07C273/18; C07C273/1809; C07D307/00; C07D307/77; C07D307/78; C07D307/86; C07D317/00; C07D317/08; C07D317/10; C07D317/14; C07D317/18; C07D317/24

Claims Analysis

Total Claims: 2
Claim 1
Independent Claim 141 words
In a process for the preparation of a compound selected from the group which consists of: 2-(1,3-dioxolane-2-yl)-phenyl-N-phenyl-carbamate; 2-(1,3-dioxolane-2-yl)-phenyl-N-methyl-carbamate; 2-(1,3-dioxolane-2-yl)-phenyl-N-3-chlorophenyl-carbamate; 2-(1,3-dioxolane-2-yl)-phenyl-N-cyclohexyl-carbamate; 2-(1,3-dioxolane-2-yl)-phenyl-N-3,4-dichlorophenyl-carbamate; 2-(1,3-dioxolane-2-yl)-phenyl-N-4-chlorophenyl-carbamate; 2,2-dimethyl-2,3-dihydro-benzofuran-7-yl-N-methyl-carbamate; 3-methyl-phenyl-N-methyl-carbamate; 2-chlorophenyl-N-methyl-carbamate; and 4-isopropylphenyl-N-methyl-carbamate by reaction of phosgene with a phenol of the formula: R.sup.2 --OH and further by the reaction of a primary amine of the formula: R.sup.1 ---NH.sub.2 wherein R 1 is selected from the group which consists of methyl, cyclohexyl, phenyl, 3-chlorophenyl, 4-chlorophenyl, and 3,4-dichlorophenyl; and R 2 is selected from the group which consists of 2-(1,3-dioxolane-2-yl)-phenyl, 3-methylphenyl, 2-chlorophenyl, 4-isopropylphenyl, and (2,3-dihydro-2,2-dimethyl-benzofuran-7-yl); the improvement which comprises reacting all three of the abovementioned reactants in a common water-immiscible organic solvent in the same reaction vessel at the same time in the presence of an acid binding agent and with about a 1:1 molar ratio of the phenol to the primary amine to yield the desired product.
Claim 2
Dependent Claim 141 words
In a process for the preparation of a compound selected from the group which consists of: 2-(1,3-dioxolane-2-yl)-phenyl-N-phenyl-carbamate; 2-(1,3-dioxolane-2-yl)-phenyl-N-methyl-carbamate; 2-(1,3-dioxolane-2-yl)-phenyl-N-3-chlorophenyl-carbamate; 2-(1,3-dioxolane-2-yl)-phenyl-N-cyclohexyl-carbamate; 2-(1,3-dioxolane-2-yl)-phenyl-N-3,4-dichlorophenyl-carbamate; 2-(1,3-dioxolane-2-yl)-phenyl-N-4-chlorophenyl-carbamate; 2,2-dimethyl-2,3-dihydro-benzofuran-7-yl-N-methyl-carbamate; 3-methyl-phenyl-N-methyl-carbamate; 2-chlorophenyl-N-methyl-carbamate; and 4-isopropylphenyl-N-methyl-carbamate by reaction of phosgene with a phenol of the formula: R.sup.2 --OH and further by the reaction of a primary amine of the formula: R.sup.1 ---NH.sub.2 wherein R 1 is selected from the group which consists of methyl, cyclohexyl, phenyl, 3-chlorophenyl, 4-chlorophenyl, and 3,4-dichlorophenyl; and R 2 is selected from the group which consists of 2-(1,3-dioxolane-2-yl)-phenyl, 3-methylphenyl, 2-chlorophenyl, 4-isopropylphenyl, and (2,3-dihydro-2,2-dimethyl-benzofuran-7-yl); the improvement which comprises reacting all three of the abovementioned reactants in a common water-immiscible organic solvent in the same reaction vessel at the same time in the presence of an acid binding agent and with about a 1:1 molar ratio of the phenol to the primary amine to yield the desired product.

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1981-04-24 1981-10-24 1982-04-25 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1985-04-24 1985-10-24 1986-04-25 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1989-04-24 1989-10-24 1990-04-25 $7700.00 Window Closed / Lapsed

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