JPS55162760A - Phenylacetamide derivative - Google Patents

Info

Publication number

JPS55162760A

JPS55162760A JP4073579A JP4073579A JPS55162760A JP S55162760 A JPS55162760 A JP S55162760A JP 4073579 A JP4073579 A JP 4073579A JP 4073579 A JP4073579 A JP 4073579A JP S55162760 A JPS55162760 A JP S55162760A

Authority

JP

Japan

Prior art keywords

formula

compound

reacted

integer

give

Prior art date

1979-04-04

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
• Discuss

• LSBDFXRDZJMBSC-UHFFFAOYSA-N 2-phenylacetamide Chemical class NC(=O)CC1=CC=CC=C1 LSBDFXRDZJMBSC-UHFFFAOYSA-N 0.000 title 1
• 150000001875 compounds Chemical class 0.000 abstract 4
• UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 3
• 125000000217 alkyl group Chemical group 0.000 abstract 2
• 238000000034 method Methods 0.000 abstract 2
• WLJVXDMOQOGPHL-UHFFFAOYSA-N phenylacetic acid Chemical compound OC(=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-UHFFFAOYSA-N 0.000 abstract 2
• XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 abstract 2
• 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 2
• BANNXMFVLBMVSD-UHFFFAOYSA-N 2-(4-methoxyphenyl)-n-[2-[methyl(oxolan-2-ylmethyl)amino]ethyl]-n-(1,2,3,4-tetrahydronaphthalen-1-ylmethyl)acetamide Chemical compound C1=CC(OC)=CC=C1CC(=O)N(CC1C2=CC=CC=C2CCC1)CCN(C)CC1OCCC1 BANNXMFVLBMVSD-UHFFFAOYSA-N 0.000 abstract 1
• VGCXGMAHQTYDJK-UHFFFAOYSA-N Chloroacetyl chloride Chemical compound ClCC(Cl)=O VGCXGMAHQTYDJK-UHFFFAOYSA-N 0.000 abstract 1
• 125000003342 alkenyl group Chemical group 0.000 abstract 1
• 125000003545 alkoxy group Chemical group 0.000 abstract 1
• 150000001412 amines Chemical class 0.000 abstract 1
• 230000000202 analgesic effect Effects 0.000 abstract 1
• 239000007795 chemical reaction product Substances 0.000 abstract 1
• 239000003795 chemical substances by application Substances 0.000 abstract 1
• 239000003814 drug Substances 0.000 abstract 1
• 229910052736 halogen Inorganic materials 0.000 abstract 1
• 150000002367 halogens Chemical class 0.000 abstract 1
• 239000000463 material Substances 0.000 abstract 1
• 239000003960 organic solvent Substances 0.000 abstract 1
• 229960003424 phenylacetic acid Drugs 0.000 abstract 1
• 239000003279 phenylacetic acid Substances 0.000 abstract 1
• 239000000047 product Substances 0.000 abstract 1
• 150000003839 salts Chemical class 0.000 abstract 1
• 239000007858 starting material Substances 0.000 abstract 1