HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1657603Generated: November 3, 2026
4-Piperidineethanol → HCID 21534829, compound
https://huagongshe.com/reaction/1657603
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Piperidineethanol | HCID 73953 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 21534822 | HCID 21534822 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21534829 | HCID 21534829 | 73.2% |
Reaction Steps
A mixture of 2-heptyloxy-6-dimethylsulphamoyl-10-(3-chloropropyl)phenothiazine (24.3 g.), 4-hydroxyethylpiperidine (7.1 g.) and sodium bicarbonate (16.1 g.) in dimethylformamide (180 cc.) is heated at about 130°C. for 8 hours with stirring. After cooling, the reaction mixture is evaporated to dryness under reduced pressure (15 mm.Hg) with heating to 65°C. The residue is taken up in distilled water (300 cc.) and then extracted with methylene chloride (total 560 cc.). The combined organic extracts are acidified by addition of a solution of methanesulphonic acid (57.6 cc.) in water (250 cc.). The organic phase is washed with an 8% aqueous solution of sodium hydroxide (total 300 cc.) and then with distilled water (total 1 litre), and is finally dried over sodium sulphate. On evaporation of the solvent under reduced pressure (15 mm. Hg) at 40°C., crude 2-heptyloxy-6-dimethylsulphamoyl-10-[3-(4-hydroxyethylpiperidino)propyl]-phenothiazine (21.1 g.), in the form of a brown viscous oil, is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03961055 |
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| Source dataset | uspto-grants-1976_06 |
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| ORD ID | ord-dddfb84a941548e199e006d8a8c4bd14 |
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| Source note | uspto-grants-1976_06 |
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