JPS55139381A - Spiroisochroman - Google Patents

Info

Publication number

JPS55139381A

JPS55139381A JP4516779A JP4516779A JPS55139381A JP S55139381 A JPS55139381 A JP S55139381A JP 4516779 A JP4516779 A JP 4516779A JP 4516779 A JP4516779 A JP 4516779A JP S55139381 A JPS55139381 A JP S55139381A

Authority

JP

Japan

Prior art keywords

formula

compound

alkyl

give

spiro

Prior art date

1979-04-13

Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)

Granted

Links

• Espacenet
• Global Dossier
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• 150000001875 compounds Chemical class 0.000 abstract 4
• 125000000217 alkyl group Chemical group 0.000 abstract 3
• LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 2
• BDQSEUUZQUPTHA-UHFFFAOYSA-N 1'-benzylspiro[1,3-dihydroisochromene-4,4'-piperidine] Chemical compound C1CC2(C3=CC=CC=C3COC2)CCN1CC1=CC=CC=C1 BDQSEUUZQUPTHA-UHFFFAOYSA-N 0.000 abstract 1
• VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 1
• DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 abstract 1
• 125000003545 alkoxy group Chemical group 0.000 abstract 1
• 239000000043 antiallergic agent Substances 0.000 abstract 1
• 125000003710 aryl alkyl group Chemical group 0.000 abstract 1
• 230000000903 blocking effect Effects 0.000 abstract 1
• KRVSOGSZCMJSLX-UHFFFAOYSA-L chromic acid Substances O[Cr](O)(=O)=O KRVSOGSZCMJSLX-UHFFFAOYSA-L 0.000 abstract 1
• 230000000694 effects Effects 0.000 abstract 1
• 238000005886 esterification reaction Methods 0.000 abstract 1
• AWJWCTOOIBYHON-UHFFFAOYSA-N furo[3,4-b]pyrazine-5,7-dione Chemical compound C1=CN=C2C(=O)OC(=O)C2=N1 AWJWCTOOIBYHON-UHFFFAOYSA-N 0.000 abstract 1
• 238000010438 heat treatment Methods 0.000 abstract 1
• 229910000041 hydrogen chloride Inorganic materials 0.000 abstract 1
• IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 abstract 1
• 125000002768 hydroxyalkyl group Chemical group 0.000 abstract 1
• 239000012280 lithium aluminium hydride Substances 0.000 abstract 1
• -1 lithium aluminum hydride Chemical compound 0.000 abstract 1
• 239000000463 material Substances 0.000 abstract 1
• 239000007800 oxidant agent Substances 0.000 abstract 1
• 230000001590 oxidative effect Effects 0.000 abstract 1
• 238000002360 preparation method Methods 0.000 abstract 1
• 229910052708 sodium Inorganic materials 0.000 abstract 1
• 239000011734 sodium Substances 0.000 abstract 1
• 150000003413 spiro compounds Chemical class 0.000 abstract 1
• LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 abstract 1

Cited By (2)