SU335246A1 - - Google Patents

Info

Publication number

SU335246A1

SU335246A1 SU1456231A SU1456231A SU335246A1 SU 335246 A1 SU335246 A1 SU 335246A1 SU 1456231 A SU1456231 A SU 1456231A SU 1456231 A SU1456231 A SU 1456231A SU 335246 A1 SU335246 A1 SU 335246A1

Authority

SU

USSR - Soviet Union

Prior art keywords

ester

aldehyde

indolyl

yield

indole

Prior art date

Links

• Espacenet
• Global Dossier
• Discuss

• LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
• -1 3-indolyl Chemical group 0.000 description 4
• 239000002253 acid Substances 0.000 description 4
• 238000000034 method Methods 0.000 description 4
• XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 4
• 150000002148 esters Chemical class 0.000 description 3
• 125000004494 ethyl ester group Chemical group 0.000 description 3
• 239000000047 product Substances 0.000 description 3
• SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 2
• 238000006243 chemical reaction Methods 0.000 description 2
• 150000001875 compounds Chemical class 0.000 description 2
• FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 2
• VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
• 239000005977 Ethylene Substances 0.000 description 1
• QIVBCDIJIAJPQS-VIFPVBQESA-N L-tryptophane Chemical compound C1=CC=C2C(C[C@H](N)C(O)=O)=CNC2=C1 QIVBCDIJIAJPQS-VIFPVBQESA-N 0.000 description 1
• DIQDUFVJZPNLJQ-UHFFFAOYSA-N N-Benzoyl-Indole Natural products C1=CC2=CC=CC=C2N1C(=O)C1=CC=CC=C1 DIQDUFVJZPNLJQ-UHFFFAOYSA-N 0.000 description 1
• 125000003047 N-acetyl group Chemical group 0.000 description 1
• QIVBCDIJIAJPQS-UHFFFAOYSA-N Tryptophan Natural products C1=CC=C2C(CC(N)C(O)=O)=CNC2=C1 QIVBCDIJIAJPQS-UHFFFAOYSA-N 0.000 description 1
• BQRAAEWJXGXLIW-UHFFFAOYSA-N [P].Cl=O Chemical compound [P].Cl=O BQRAAEWJXGXLIW-UHFFFAOYSA-N 0.000 description 1
• 230000015572 biosynthetic process Effects 0.000 description 1
• 238000006073 displacement reaction Methods 0.000 description 1
• 238000009472 formulation Methods 0.000 description 1
• PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 description 1
• RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 description 1
• 238000002955 isolation Methods 0.000 description 1
• 238000004519 manufacturing process Methods 0.000 description 1
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
• 239000000203 mixture Substances 0.000 description 1
• 239000002243 precursor Substances 0.000 description 1
• 238000002360 preparation method Methods 0.000 description 1
• 239000012265 solid product Substances 0.000 description 1
• 239000000725 suspension Substances 0.000 description 1
• 238000003786 synthesis reaction Methods 0.000 description 1