JPS5668668A - Preparation of 2-indolinones - Google Patents

Info

Publication number

JPS5668668A

JPS5668668A JP14471679A JP14471679A JPS5668668A JP S5668668 A JPS5668668 A JP S5668668A JP 14471679 A JP14471679 A JP 14471679A JP 14471679 A JP14471679 A JP 14471679A JP S5668668 A JPS5668668 A JP S5668668A

Authority

JP

Japan

Prior art keywords

copper

lower alkyl

compound

formula

aqueous ammonia

Prior art date

1979-11-08

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

• JYGFTBXVXVMTGB-UHFFFAOYSA-N indolin-2-one Chemical class C1=CC=C2NC(=O)CC2=C1 JYGFTBXVXVMTGB-UHFFFAOYSA-N 0.000 title abstract 3
• 125000000217 alkyl group Chemical group 0.000 abstract 3
• VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 abstract 2
• RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 abstract 2
• 239000005749 Copper compound Substances 0.000 abstract 2
• 239000002253 acid Substances 0.000 abstract 2
• 125000003545 alkoxy group Chemical group 0.000 abstract 2
• QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract 2
• 229910052802 copper Inorganic materials 0.000 abstract 2
• 239000010949 copper Substances 0.000 abstract 2
• 150000001880 copper compounds Chemical class 0.000 abstract 2
• 150000002148 esters Chemical class 0.000 abstract 2
• IUJAAIZKRJJZGQ-UHFFFAOYSA-N 2-(2-chlorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC=C1Cl IUJAAIZKRJJZGQ-UHFFFAOYSA-N 0.000 abstract 1
• 125000003342 alkenyl group Chemical group 0.000 abstract 1
• 150000001875 compounds Chemical class 0.000 abstract 1
• ORTQZVOHEJQUHG-UHFFFAOYSA-L copper(II) chloride Chemical compound Cl[Cu]Cl ORTQZVOHEJQUHG-UHFFFAOYSA-L 0.000 abstract 1
• QYCVHILLJSYYBD-UHFFFAOYSA-L copper;oxalate Chemical compound [Cu+2].[O-]C(=O)C([O-])=O QYCVHILLJSYYBD-UHFFFAOYSA-L 0.000 abstract 1
• 229910052736 halogen Inorganic materials 0.000 abstract 1
• 125000005843 halogen group Chemical group 0.000 abstract 1
• 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
• 239000000575 pesticide Substances 0.000 abstract 1
• 239000002994 raw material Substances 0.000 abstract 1
• 238000007363 ring formation reaction Methods 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 (1)