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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D285-10
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D285-10
filingDate 1971-08-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1973-02-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_269b23f872dcd5ddbddde44424fdefe5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f24b056b57bd7107fefb9ebf862dca8f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_04e5ea37d1e8a3ef0b1b7a9e409c3df8
publicationDate 1973-02-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-3718647-A
titleOfInvention Process for making 1,2,5-thiadiazoles in the sinister configuration and novel intermediates
abstract PREPARATION OF S-3-X-4-(3-SUBTITUTED AMINO-2-HYDROXYPROPOXY)-1,2,5-THIADIAZOLE BETA ADRENERGIC BLOCKING AGENTS USING AS STARING MATERIAL AN OPTICALLY ACTIVE ALKAMINE IN THE SINSTER CONFIGURATION, OR A DERIVATIVE OF SAID ALKAMINE, WHICH IS REACTED WITH AN 3-X-4-CHLORO(OR RO- WHERE R IS HYDROGEN OR AN ALKALI METAL9-1,2,5THIADIAZOLE. NOVEL 3-MORPHOLINO-4-CHLORO(OR RO-)1,2,5-THIADIAZOLES AND NOVEL ALKAMINES AND THEIR PREPARATION ALSO ARE DESCRIBED.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4178374-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4238485-A
priorityDate 1971-08-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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