http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2005220129-A

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http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_24aca9ded2638ea793d05360dde7a4a0
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C273-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C275-14
filingDate 2005-01-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f1e50db33ed22481e4ade76068e9f210
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dd4fcd5073797b9c3956d80d8e72e75f
publicationDate 2005-08-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2005220129-A
titleOfInvention Method for producing methylurea compound
abstract The present invention relates to formula (2) without using methyl isocyanate, which is problematic in terms of availability and safety. A process for producing a methylurea compound represented by the formula (1) with high selectivity. (A) Formula (1) (In the formula, Ar represents an aromatic group which may be substituted with a substituent other than an amino group, and n represents an integer of 1 to 3). A step of reacting an N-methylcarbamic acid compound represented by the formula (2) with an excess amount of ethylenediamine to obtain a reaction solution containing the methylurea compound represented by the formula (2) and unreacted ethylenediamine, (B) a step of concentrating the reaction solution to remove ethylenediamine in the reaction solution and taking out a methylurea compound represented by the formula (2); A process for producing a methylurea compound, comprising: [Selection figure] None
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-11352319-B2
priorityDate 2004-01-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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