http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-3770767-A

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grantDate 1973-11-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8990ee421aba24cb0f1e1b51218290d0
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publicationDate 1973-11-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-3770767-A
titleOfInvention 2-aminomethylindole derivatives
abstract BENZODIAZEPINE DERIVATIVES, WHICH HAVE BEEN WELL KNOWN AS EXCELLENT TRANQUILIZERS AND WHICH HAVE THE FORMULA 5-(X-C6H4-),2-(O=),1-R,(O2N-)-1,2-DIHYDRO-3H-1,4- WHEREIN R SIGNIFIES A METHYL, ETHYL OR THE LIKE GROUP; AND X SIGNIFIES A HYDROGEN, CHLORINE OR THE LIKE ATOM, ARE OBTAINED BY REACTING WITH AN OXIDIZING AGENT, SUCH AS CHROMIC ACID OR THE LIKE, A NOVEL 2-AMOINMETHYLINDOLE DERIVATIVE OF THE FORMULA: BENZODIAZEPINE WHEREIN X HAS THE SAME SIGNIFICANCE AS MENTIONED ABOVE, SUBJECTING SAID DERIVATIVE TO N-ALKYLATION, HYDROLYSIS, AND AMIDATION TO FORM A CORRESPONDING ACID AMIDE, DEHYDRATING SAID ACID AMIDE TO A CORRESPONDING CARBONITRILE, AND THEN REDUCING SAID CARBONITRILE. 2-(C2H5-OOC-),3-(X-C6H4-),(O2N-)INDOLE WHEREIN X HAS THE SAME SIGNIFICANCE AS MENTIONED ABOVE, TO FORM AN IDOLE-2-CARBOXYLIC ACID ESTER DERIVATIVE OF THE FORMULA: X-C6H4-CH2-CH(-COO-C2H5)-CO-CH3 WHEREIN Y SIGNIFIES A HALOGEN ATOM, WITH AN ESTER OF BKETO-ACID OF THE FORMULA: O2N-C6H4-N2(+) Y(-) WHEREIN R AND X HAVE THE SAME SIGNIFICANCES AS MENTIONED ABOVE, OR ITS SALT. THE STARTING 2-AMINOMETHYLINDOLE DERIVATIVE IS PREPARED BY REACTING A NITROBENZENDEDIAZONIUM DERIVATIVE OF THE FORMULA: 1-R,2-(NH2-CH2-),3-(X-C6H4-),(O2N-)INDOLE
priorityDate 1967-12-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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