SU411087A1 - - Google Patents

Info

Publication number

SU411087A1

SU411087A1 SU1732561A SU1732561A SU411087A1 SU 411087 A1 SU411087 A1 SU 411087A1 SU 1732561 A SU1732561 A SU 1732561A SU 1732561 A SU1732561 A SU 1732561A SU 411087 A1 SU411087 A1 SU 411087A1

Authority

SU

USSR - Soviet Union

Prior art keywords

benzene

pyridine

residue

sulfur atom

organic solvent

Prior art date

1971-12-31

Links

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• UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 20
• JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 9
• 238000000034 method Methods 0.000 claims description 9
• 238000009835 boiling Methods 0.000 claims description 5
• -1 isoindolinylideneamino Chemical group 0.000 claims description 4
• UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 4
• 229910052717 sulfur Inorganic materials 0.000 claims description 4
• 125000004434 sulfur atom Chemical group 0.000 claims description 4
• 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims description 3
• 239000003960 organic solvent Substances 0.000 claims description 3
• 125000003118 aryl group Chemical group 0.000 claims description 2
• 125000000732 arylene group Chemical group 0.000 claims 1
• LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 24
• 150000001875 compounds Chemical class 0.000 description 8
• LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
• YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
• 239000000047 product Substances 0.000 description 5
• 238000010521 absorption reaction Methods 0.000 description 4
• 238000001816 cooling Methods 0.000 description 4
• 239000002244 precipitate Substances 0.000 description 4
• 238000010992 reflux Methods 0.000 description 4
• 238000003756 stirring Methods 0.000 description 3
• 238000006243 chemical reaction Methods 0.000 description 2
• 238000002360 preparation method Methods 0.000 description 2
• VHNQIURBCCNWDN-UHFFFAOYSA-N pyridine-2,6-diamine Chemical compound NC1=CC=CC(N)=N1 VHNQIURBCCNWDN-UHFFFAOYSA-N 0.000 description 2
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
• NQBUVYWRXKJRRR-UHFFFAOYSA-N 4-(4-benzhydrylpiperazin-1-yl)-1-phenylpyrazolo[3,4-d]pyrimidine Chemical compound C1CN(C=2C=3C=NN(C=3N=CN=2)C=2C=CC=CC=2)CCN1C(C=1C=CC=CC=1)C1=CC=CC=C1 NQBUVYWRXKJRRR-UHFFFAOYSA-N 0.000 description 1
• 150000004982 aromatic amines Chemical class 0.000 description 1
• 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
• 230000003993 interaction Effects 0.000 description 1
• 238000002955 isolation Methods 0.000 description 1
• 238000004519 manufacturing process Methods 0.000 description 1
• 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
• 238000003786 synthesis reaction Methods 0.000 description 1