JPS5531071A - Preparation of indenothiophene derivative - Google Patents

Info

Publication number

JPS5531071A

JPS5531071A JP9487179A JP9487179A JPS5531071A JP S5531071 A JPS5531071 A JP S5531071A JP 9487179 A JP9487179 A JP 9487179A JP 9487179 A JP9487179 A JP 9487179A JP S5531071 A JPS5531071 A JP S5531071A

Authority

JP

Japan

Prior art keywords

formula

compound

indeno

thiophen

subjected

Prior art date

1979-07-27

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

• RNXIRXYZZGOBQG-UHFFFAOYSA-N 2h-indeno[2,1-b]thiophene Chemical class C1=CC=C2C3=CCSC3=CC2=C1 RNXIRXYZZGOBQG-UHFFFAOYSA-N 0.000 title 1
• 150000001875 compounds Chemical class 0.000 abstract 4
• 239000000463 material Substances 0.000 abstract 4
• HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract 3
• 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 2
• 229910052736 halogen Inorganic materials 0.000 abstract 2
• 125000005843 halogen group Chemical group 0.000 abstract 2
• 238000000034 method Methods 0.000 abstract 2
• 238000006798 ring closing metathesis reaction Methods 0.000 abstract 2
• FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-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
• YCYPIWSUCIXKEB-UHFFFAOYSA-N 2-bromo-6,8-dinitroindeno[1,2-b]thiophen-4-one Chemical compound [O-][N+](=O)C1=CC([N+](=O)[O-])=CC2=C1C(SC(Br)=C1)=C1C2=O YCYPIWSUCIXKEB-UHFFFAOYSA-N 0.000 abstract 1
• 239000002841 Lewis acid Substances 0.000 abstract 1
• 239000012024 dehydrating agents‎ Substances 0.000 abstract 1
• WSOJIQBCVMSHLB-UHFFFAOYSA-N indeno[1,2-b]thiophen-4-one Chemical class C12=CC=CC=C2C(=O)C2=C1SC=C2 WSOJIQBCVMSHLB-UHFFFAOYSA-N 0.000 abstract 1
• 150000007517 lewis acids Chemical class 0.000 abstract 1
• 229920003227 poly(N-vinyl carbazole) Polymers 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