http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CH-501633-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_12cedce8d26d81271038993ba4912fe6 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D493-08 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D493-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-08 |
| filingDate | 1967-04-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_94f139c3e8a10bff9ed1176d448af31d http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5945714757b40db59c6505bd7dde3654 |
| publicationDate | 1971-01-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CH-501633-A |
| titleOfInvention | Process for the preparation of 10,5- (iminomethanol) -10,11-dihydro-5H-dibenzo (a, d) cycloheptene derivatives |
| abstract | (A) Cpds. of general formula (I) R and R' = H, (1-4C) alkyl, unsat. lower alkyl, opt. subst. (7-10C)aralkyl, (4-9C)N(alkyl)2, heteroalkyl with (5-8C) and (1-2 hetero) atoms, (2-4C)aliphatic acyl, (7-10C)-aroyl, or (8-12C)aralkanoyl and R2 = (1-4C)alkyl, unsat. lower alkyl, Ph, opt. subst. (7-10C) aralkyl, or (5-9C)N(alkyl)2. (B) Acid addn. salts of I. (a) Trichomonacides (b) Antiparasitics (c) Anti-cramp (d) Anti-inflammatories (e) Hypotensives. Br2 (10.3 ml.) in CHCl3 (100 ml.) was added dropwise (2 h.) to 5H-dibenzo(a,d)cycloheptene-5-carboxamide (47.0 g.) in CHCl3(1 l.), stored overnight, and filtered. The solid was refluxed 2 h. in EtOH (200 ml.) and H2O (10 ml.), evapd., washed with H2O, and recryst. from EtOH, giving the 10,5-epoxymethano-13-one m.p. 160-1 deg. |
| priorityDate | 1966-04-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 143.