http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H11302234-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C247-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C215-44
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C213-02
filingDate 1998-04-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7a6dee79206c4cc5cc08ed8867436553
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f9615350328837fd10ceb2dde8a1c762
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_34b1b326993f34fa9bc9714b91403cac
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publicationDate 1999-11-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H11302234-A
titleOfInvention Method for producing aminoindanol
abstract PROBLEM TO BE SOLVED: To provide a process for producing cis-1-amino-2-indanol, and cis-1-azide-2 which is an intermediate of the compound -Provision of a method for producing indanol [Solution] Formula (1) [In the formula, X represents a halogen atom, and the OH group and the X group are in a trans configuration, and may be a racemic form or an optically active form. And a trans-1-halo-2-indanol represented by the formula (2): [Wherein, M represents an alkali metal element. And a metal azide represented by the formula (3): [In the formula, the OH group and the N3 group have a cis configuration, and may be a racemic form or an optically active form. Cis-1-azido-2-indanol represented by the formula (4), and further reducing the compound represented by the formula (3): [In the formula, the OH group and the NH 2 group have a cis configuration, and may be a racemic form or an optically active form. The method for producing cis-1-amino-2-indanol represented by the formula:
priorityDate 1998-04-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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