JPS56164157A - Novel-alpha-oxyphenylacetamide derivative - Google Patents

Info

Publication number

JPS56164157A

JPS56164157A JP6757380A JP6757380A JPS56164157A JP S56164157 A JPS56164157 A JP S56164157A JP 6757380 A JP6757380 A JP 6757380A JP 6757380 A JP6757380 A JP 6757380A JP S56164157 A JPS56164157 A JP S56164157A

Authority

JP

Japan

Prior art keywords

alkyl

formula

derivative

compound

oxyphenylacetamide

Prior art date

1980-05-20

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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• 125000000217 alkyl group Chemical group 0.000 abstract 4
• UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 3
• YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract 3
• 150000001875 compounds Chemical class 0.000 abstract 2
• XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 abstract 2
• NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 abstract 1
• -1 N-2( N, N-Dimethylamino )ethyl-N- 2-phenylethyl- α-hydroxyphenylacetamide Chemical compound 0.000 abstract 1
• 239000002253 acid Substances 0.000 abstract 1
• 125000003342 alkenyl group Chemical group 0.000 abstract 1
• 125000003545 alkoxy group Chemical group 0.000 abstract 1
• 150000008064 anhydrides Chemical class 0.000 abstract 1
• 239000000730 antalgic agent Substances 0.000 abstract 1
• 239000003795 chemical substances by application Substances 0.000 abstract 1
• 125000002768 hydroxyalkyl group Chemical group 0.000 abstract 1
• 238000002347 injection Methods 0.000 abstract 1
• 239000007924 injection Substances 0.000 abstract 1
• IWYDHOAUDWTVEP-UHFFFAOYSA-N mandelic acid Chemical compound OC(=O)C(O)C1=CC=CC=C1 IWYDHOAUDWTVEP-UHFFFAOYSA-N 0.000 abstract 1
• OHZZTXYKLXZFSZ-UHFFFAOYSA-I manganese(3+) 5,10,15-tris(1-methylpyridin-1-ium-4-yl)-20-(1-methylpyridin-4-ylidene)porphyrin-22-ide pentachloride Chemical compound [Cl-].[Cl-].[Cl-].[Cl-].[Cl-].[Mn+3].C1=CN(C)C=CC1=C1C(C=C2)=NC2=C(C=2C=C[N+](C)=CC=2)C([N-]2)=CC=C2C(C=2C=C[N+](C)=CC=2)=C(C=C2)N=C2C(C=2C=C[N+](C)=CC=2)=C2N=C1C=C2 OHZZTXYKLXZFSZ-UHFFFAOYSA-I 0.000 abstract 1
• 239000000463 material Substances 0.000 abstract 1
• 238000000034 method Methods 0.000 abstract 1
• 150000003839 salts Chemical class 0.000 abstract 1
• 239000002904 solvent Substances 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