JPS5673083A - Novel benzopyran derivative - Google Patents

Info

Publication number

JPS5673083A

JPS5673083A JP15035579A JP15035579A JPS5673083A JP S5673083 A JPS5673083 A JP S5673083A JP 15035579 A JP15035579 A JP 15035579A JP 15035579 A JP15035579 A JP 15035579A JP S5673083 A JPS5673083 A JP S5673083A

Authority

JP

Japan

Prior art keywords

formula

compound

vacuo

solvent

benzopyran derivative

Prior art date

1979-11-19

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

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• 150000001562 benzopyrans Chemical class 0.000 title abstract 2
• XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 abstract 3
• CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 abstract 2
• JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract 2
• CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 abstract 2
• UCMIRNVEIXFBKS-UHFFFAOYSA-N beta-alanine Chemical group NCCC(O)=O UCMIRNVEIXFBKS-UHFFFAOYSA-N 0.000 abstract 2
• 150000001875 compounds Chemical class 0.000 abstract 2
• 150000003839 salts Chemical class 0.000 abstract 2
• 239000002904 solvent Substances 0.000 abstract 2
• DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Natural products NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 abstract 1
• 239000004471 Glycine Substances 0.000 abstract 1
• VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 1
• KZSNJWFQEVHDMF-BYPYZUCNSA-N L-valine Chemical group CC(C)[C@H](N)C(O)=O KZSNJWFQEVHDMF-BYPYZUCNSA-N 0.000 abstract 1
• KZSNJWFQEVHDMF-UHFFFAOYSA-N Valine Chemical group CC(C)C(N)C(O)=O KZSNJWFQEVHDMF-UHFFFAOYSA-N 0.000 abstract 1
• 239000002253 acid Substances 0.000 abstract 1
• 238000013019 agitation Methods 0.000 abstract 1
• 125000000217 alkyl group Chemical group 0.000 abstract 1
• 230000000845 anti-microbial effect Effects 0.000 abstract 1
• 229940000635 beta-alanine Drugs 0.000 abstract 1
• 230000003327 cancerostatic effect Effects 0.000 abstract 1
• 239000003795 chemical substances by application Substances 0.000 abstract 1
• 238000001816 cooling Methods 0.000 abstract 1
• 239000003814 drug Substances 0.000 abstract 1
• 125000003630 glycyl group Chemical group [H]N([H])C([H])([H])C(*)=O 0.000 abstract 1
• 229910052736 halogen Inorganic materials 0.000 abstract 1
• 125000005843 halogen group Chemical group 0.000 abstract 1
• 229910052943 magnesium sulfate Inorganic materials 0.000 abstract 1
• 235000019341 magnesium sulphate Nutrition 0.000 abstract 1
• 239000000463 material Substances 0.000 abstract 1
• 238000000034 method Methods 0.000 abstract 1
• 239000012044 organic layer Substances 0.000 abstract 1
• UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 abstract 1
• 235000017550 sodium carbonate Nutrition 0.000 abstract 1
• 229910000029 sodium carbonate Inorganic materials 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
• 239000004474 valine Chemical group 0.000 abstract 1
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1