http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CH-500976-A
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_3e9445e5e3626f36e932c6451a928250 |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D207-32 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D207-32 |
filingDate | 1968-04-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6b492400233f1f252888d7b41a2cc254 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_648934ca7818a9c1186ddf388032a877 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4095765aabc7febde624c1a24cfe4c52 |
publicationDate | 1970-12-31-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | CH-500976-A |
titleOfInvention | Process for the preparation of new, substituted phenylalkanoic acids |
abstract | (A) Cpds. of general formula (I) Z=CH2 or CO R1=H, F, Cl, or Br (B) Salts of I (II). (C) Some cpds. (IV). Analgesics, antiphlogistics, and antipyretics. Dose 50-3000 mg. 4-(p-(1-pyrryl)phenyl)butyronitrile (3.4 g), NaOH (3.3 g), EtOH (30 ml) and H2O (10 ml), were refluxed 18 hr., evapd. in vac., taken up in H2O (30 ml), and extd. with Et2O (70 ml). The H2O phase was sepd., acidified at 0 deg. with c. HCl (7 ml), filtered, washed with ice-water (5 ml), and dried, and the crude product (3.0 g) recryst. from PriOH, giving I, 113-4 deg. |
priorityDate | 1968-04-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 61.