http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H04270272-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_e45efeaa6a34dfd9d44fa29a7fe0c806 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D265-30 |
| filingDate | 1991-02-25-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d7cf709224afdd65c1bd66f5a9b6dc1b http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8351efd827c6583f36c1485fd117b2fe http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_eb1d2fde6c72c5ce09f54e58ea0e5904 |
| publicationDate | 1992-09-25-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-H04270272-A |
| titleOfInvention | Production of aminoalkylmorpholine derivative |
| abstract | PURPOSE: To obtain the title compound as an intermediate for medicines safely and in high yield by Hoffmann reaction with a readily available and novel carbamoylmorpholine derivative. n CONSTITUTION: A compound of formula I (R is alkyl, aralkyl, acyl, etc.; (n) is 1-3) is put to Hoffmann reaction and, if needed, to deprotecting reaction into the objective compound of formula II[R' is H, alkyl, aralkyl, etc.; R 1 is H or COOR 2 (R 2 is alkyl or aralkyl)]. The Hoffmann reaction can be performed in the presence of e.g. sodium hypochlorite in a solvent such as water or an alcohol (e.g. methanol, ethanol) at -30 to 200 (pref. 0-100)°C. n COPYRIGHT: (C)1992,JPO&Japio |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2005525390-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-9422843-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2004509953-A |
| priorityDate | 1991-02-25-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 25.