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N,N,N-trisubstituted N-halogenomethylurea and thiourea compounds and process for their preparation

Assignee: Bayer AG
•
Filing: 1973-02-21
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Granted: 1976-01-06
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Expires: 1993-02-21
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Abstract

Abstract Novel N,N',N'-trisubstituted N-halogenomethylurea compounds of the formula: ##EQU1## in which R 1 is alkyl, cycloalkyl, cycloalkenyl, bicycloalkyl, bicycloalkenyl, aryl or aralkyl (each of which may be optionally substituted), R 2 is alkyl, alkenyl, alkynyl or alkoxy (each of which may be optionally substituted), or halogenoalkyl or cycloalkyl, R 3 is alkyl (which may be optionally halogen-substituted), alkenyl or alkynyl, or R 2 and R 3 jointly represent an alkylene bridge which, can be interrupted by one or more hetero-atoms, such as S or O, or by the NH group, and which forms a heterocyclic ring with the adjoining nitrogen atom, X is oxygen or sulfur, and Y is chlorine or bromine. Are prepared by reacting a N,N',N'-trisubstituted urea or thiourea of the general formula: ##EQU2## in which R 1 , R 2 , R 3 and X have the above-mentioned meanings, is reacted, per mole thereof, with at least 1 mole of formaldehyde (which may be formed in situ from a formaldehyde-releasing substance) and a halogenating agent at a temperature of from -10° to +150°C, optionally in the presence of a diluent and, as a catalyst, a proton-releasing compound (for example a hydrogen halide) or a Lewis acid.

Inventors

  • 👤 Rudolf Thomas
  • 👤 Wolfgang Kramer
  • 👤 Ludwig Eue
  • 👤 Carl Metzger
  • 👤 Gerhard Jager

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-08 13:30
CPC Classifications
C; C07; C07C; C07C275/00; C07C275/64; C07C273/00; C07C273/18; C07C273/1854; C07C275/28; C07C275/30; C07C275/32; C07C275/34; C07C335/00; C07C335/04; D; D06; D06P; D06P1/00; D06P1/44; D06P1/64; D06P1/642; D06P1/649; D06P1/6491

Claims Analysis

Total Claims: 8
Claim 1
Independent Claim 55 words
N,N',N'-trisubstituted N-halogenomethylurea compound of the formula ##EQU12## in which X is oxygen or sulfur R 1 is phenyl, unsubstituted or substituted with chlorine, bromine, trifluoromethyl, trifluoromethoxy, nitro, methyl, ethyl, methoxy, methylthio, ethoxy or chlorophenoxy, R 2 and R 3 are selected from the group of methyl, butyl, allyl, ##EQU13## and chloroethyl, and Y is chlorine.
Claim 2
Dependent Claim 55 words
N,N',N'-trisubstituted N-halogenomethylurea compound of the formula ##EQU12## in which X is oxygen or sulfur R 1 is phenyl, unsubstituted or substituted with chlorine, bromine, trifluoromethyl, trifluoromethoxy, nitro, methyl, ethyl, methoxy, methylthio, ethoxy or chlorophenoxy, R 2 and R 3 are selected from the group of methyl, butyl, allyl, ##EQU13## and chloroethyl, and Y is chlorine.
Claim 3
Dependent Claim 27 words
Compound as claimed in claim 1 wherein R 1 is 4-chlorophenyl or 3,4-dichlorophenyl, R 2 and R 3 are methyl, X is sulfur and Y is chlorine.
Claim 4
Dependent Claim 28 words
Compound as claimed in claim 1 wherein R 1 is 4-chlorophenyl or 3,4-dichlorophenyl, R 2 is methoxy, R 3 is methyl, X is oxygen, and Y is chlorine.
Claim 5
Dependent Claim 8 words
Compound as claimed in claim 1 designated 1-chloromethyl-1-phenyl-3,3-dimethylurea.
Claim 6
Dependent Claim 8 words
Compound as claimed in claim 1 designated 1-chloromethyl-1-(3,4-dichlorophenyl)-3-methoxy-3-methylurea.
Claim 7
Dependent Claim 8 words
Compound as claimed in claim 1 designated 1-chloromethyl-(4-chlorophenyl)-3,3-dimethylurea.
Claim 8
Dependent Claim 8 words
Compound as claimed in claim 1 designated 1-chloromethyl-1-(3,4-dichlorophenyl)-3,3-dimethylurea.

References Cited (Backward Citations)

US3505454A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1979-01-05 1979-07-07 1980-01-06 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1983-01-05 1983-07-07 1984-01-06 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1987-01-05 1987-07-07 1988-01-06 $7700.00 Window Closed / Lapsed

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