HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → HCID 11531111, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 4-Methoxybenzenesulfonyl chloride | HCID 7401 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 11085189 | HCID 11085189 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 11531111 | HCID 11531111 | — |
Reaction Steps
4-methoxy benzene sulphonyl chloride (495 gm, 2.4 mmol) in dry acetone (5 ml) was added to a stirred solution of dl 1,2,3,4-tetrahydro-9H-pyrido(3,4-b)indole-3-amide (0.430 gm, 1.0 mmol) and dry triethylamine (0.56 ml, 4.0 mmol) in dry DMF (5 ml) during 15 min and was allowed to stirr for 8 hrs. at room temperature (32° C.). Water was added to the reaction mixture and triturated to give 2-[4-methoxybenzenesulfonyl]-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=0.480 gm, (62.34%). m.p.=178-180° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07601838B2 |
| Source dataset | uspto-grants-2009_10 |
| ORD ID | ord-55ce4a929a5c46029fd69b02e6024732 |
| Source note | uspto-grants-2009_10 |