http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H10147593-A
Outgoing Links
Predicate | Object |
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assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_6c8d4dc7bd1a30d8fda907fceaeb4e69 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07J75-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07J41-00 |
filingDate | 1996-11-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_72f67c0af12eba22ad414bf67f0a78c0 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e8ee0e0d4c87d5385c2ce24fe7087958 |
publicationDate | 1998-06-02-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | JP-H10147593-A |
titleOfInvention | Method for producing 3-aminosteroid derivative |
abstract | PROBLEM TO BE SOLVED: To provide a method for easily producing a 3-aminosteroid derivative useful as an intermediate for synthesizing a drug in a high yield. SOLUTION: (a) General formula (1) [Wherein, R 1 represents an alkyl group having 1 to 4 carbon atoms, an alkyl group having 1 to 10 carbon atoms which may have a specific substituent, and R 2 represents α-OH or β-OH Represented by the general formula (2) Is obtained by reacting with a hydrazine hydrate or phenylhydrazine to obtain a 3-phthalimide steroid derivative represented by the general formula (3): (Wherein R 1 is as defined in formula (1); 3 represents α-NH 2 or β-NH 2 ), and the resulting compound is treated with a solution of an organic acid or a mineral acid to obtain an organic acid or a mineral acid. And then converted to the free compound. |
priorityDate | 1996-11-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 52.