http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2002220381-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_2f8cfa5aee4410611b5c562275c9f8e3
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D291-06
filingDate 2001-01-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b1a1dab3fa2bb78d6d863ee6d27ea4f4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_03b1daebe883778ffd8b25f84614e64c
publicationDate 2002-08-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2002220381-A
titleOfInvention Process for producing 3,4-dihydro-1,2,3-oxathiazines or salts thereof
abstract PROBLEM TO BE SOLVED: To provide a method capable of industrially advantageously producing 3,4-dihydro-1,2,3-oxathiazine or a salt thereof. SOLUTION: In the present invention, a sulfonic acid represented by the following formula (1) is subjected to a cyclization dehydration reaction in the presence of an acid anhydride to give a 3,4-dihydro- represented by the following formula (2). 1, Produce 2,3-oxathiazines or salts thereof. As the acid anhydride, an acid anhydride composed of at least one selected from sulfonic acid, halogenated sulfuric acid, pyrophosphoric acid, nitric acid and boric acid is used. Embedded image (Wherein R 1 and R 2 are the same or different and each represent a hydrogen atom or a reaction-inactive organic group, and R 3 binds to a hydrogen atom, a reaction-inactive organic group, or a nitrogen atom to form a salt. And X represents an organic or inorganic base which forms a salt with a hydrogen atom or a sulfonate group.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-11724994-B2
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-11731948-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-107868064-A
priorityDate 2001-01-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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