http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-753573-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_73ee0bacab5a7576a6a3244747f6ea99
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D231-56
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D231-56
filingDate 1953-06-17^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d39589a7cefd467a2a6f27b4f317351a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5668a98d18166cfb287be210bd828279
publicationDate 1956-07-25^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-753573-A
titleOfInvention New dyestuffs intermediates
abstract The invention comprises indazolyl-pyrazole derivatives of the formula <FORM:0753573/IV(a)/1> where X is O or NH and Y is H or sulphonic acid. These are made from amino-indazoles or amino-indazole-sulphonic acids by diazotizing, reducing to the hydrazines, condensing the latter with acetoacetic ester, diketene and ammonia, or diacetonitrile, and ring-closing the product with caustic alkali. The products are intermediates for azo dyestuffs. Examples show the production of 1-(61-indazolyl)-3-methyl - 5 - pyrazolone, 1 - (51 - indazolyl)-3 - methyl - 5 - pyrazolone, 1 - (61 - indazolyl)-3 - methyl - 5 - aminopyrazole and 1 - (41-sulpho-61-indazolyl)-3-methyl-5-pyrazolone.
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AP-1025-A
priorityDate 1953-06-17^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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