http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2006028110-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D209-48
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D405-06
classificationIPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D405-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-48
filingDate 2004-07-20^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3981062d46b8d58c821b095eea20efef
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_645cfbf9e26f97d7df052b0f34fc9ed5
publicationDate 2006-02-02^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2006028110-A
titleOfInvention Process for producing 1-amido-3- (2-hydroxyphenoxy) -2-propanol derivatives and 2-amidomethyl-1,4-benzodioxane derivatives
abstract PROBLEM TO BE SOLVED: To provide a 1-amido-3- (2-hydroxyphenoxy) -2-propanol derivative important as a synthetic intermediate for pharmaceuticals and physiologically active substances and an optically active substance thereof. The following formula (1) (In the formula, ring A may further have 1 to 4 substituents, and the substituents are alkyl group, aralkyl group, aromatic group, halogen, halogenated alkyl group, alkanoyl group, alkylcarbamoyl group. , A cyano group, or a nitro group, and the ring A may be a condensed polycyclic hydrocarbon, R 1 represents an alkanoyl group or an aroyl group, and R 2 represents hydrogen, alkanoyl. 1-amido-3- (2-hydroxyphenoxy) -2 represented by a group or an aroyl group, or R 1 and R 2 may be bonded to form a cyclic imide group together with an N atom. -Propanol derivatives. [Selection figure] None
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2017514836-A
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