http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0050790-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c7ad58d3c0b071069a8ee0cb8c8ba2e8
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D241-44
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07B39-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D241-44
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B39-00
filingDate 1981-10-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cec3d6af76ddaccd84672ec93c489c9a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_829a2ca22f14416c538f7e2d65578467
publicationDate 1982-05-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0050790-A1
titleOfInvention Preparation of alpha-chlorinated nitrogen heterocycles
abstract Nitrogen heterocycles which contain at least one chlorine atom in the a-position to the ring nitrogen are obtained by reacting nitrogen heterocycles which contain at least one hydroxyl group in the a-position to the ring nitrogen with thionyl chloride in the presence of substituted formamides. The formamides used are N, N'-di-substituted, where both substituents independently of one another denote alkyl, aralkyl or aryl, where, in the event that both substituents denote alkyl, at least one of the two substituents contains at least 5 carbon atoms, furthermore in the alkyl substituents one or more CH 2 groups can be replaced by oxygen or alkyl or formyl-substituted nitrogen. The process is carried out in the presence of 0.001 to 1 mole of substituted formamide per mole of hydroxyl group to be reacted and at a temperature of 50 to 200 ° C.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0622360-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5777119-A
priorityDate 1980-10-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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