Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Mesitylenesulfonyl chloride | HCID 13046 | — |
| Reactant | HCID 11085189 | HCID 11085189 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 11553030 | HCID 11553030 | — |
Reaction Steps
2,4,6trimethyl benzene sulphonyl chloride (0.524 gm, 2.4 mmol) in dry acetone was added to a stirred solution of dl 1,2,3,4-tetrahydro-9H-pyrido(3,4-b)indole-3-amide (0.430 gm, 2.0 mmol) and dry triethylamine (0.56 ml, 4.0 mmol) in dry DMF (8 ml) during 15 and was allowed to stirr for 8 hrs. at room temperature. Water (20 ml) was added to the reaction mixture and extracted with chloroform (3×15 ml). The tract was dried over Na2SO4 and concentrated over reduced pressure to give 2-[2,4,6trimethylbenzenesulfonyl]-1,2,3,4,-tetrahydro-9H-pyrido[3,4-b]indole-3-carboxylic acid amide which was purified by column chromatography over silica gel using 2% methanol chloroform as eluent Yield=0.35 gm (44.08%) m.p.=212° C.: Mass (FAB) m/z=398 (M+). IR (KBr cm−1): 3394, 3299, 1668, 1596, 1455, 1324, 1155, 752. H1NMR (200 MHz, DMSO d6) δ 2.30 (s, 3H), δ2.56-2.74 (m, 7H), δ3.55-3.62 (d, 1H), δ4.49-4.70 (m, 3H), δ5.17 (s, 1H), δ5.49 (s, 1H), δ6.96-7.77 (m, 6H). Molecular Formula=C21H23N3O3S.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07601838B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-a2da235626424e9a9e51c9eef690b6c3 |
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| Source note | uspto-grants-2009_10 |
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