Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 23593636 | HCID 23593636 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 21925663 | HCID 21925663 | 127.8% |
Reaction Steps
3-(2-Chlorophenothiazin-10-yl) piperidine-1-carboxylic acid tert-butyl ester (4.1 g, 9.83 mmol) was dissolved in diethyl ether (200 mL), and the solution cooled to 0° C. A solution of HCl in ethyl acetate (˜4 M, 30 mL) was slowly added. The mixture was allowed to warn to room temperature and stirred for 8 h. The solvent was removed under vacuum. The residue treated with HCl in ethyl acetate (˜4 M, 75 mL) and stirred overnight. The solvent was removed under vacuum to provide 2-chloro-10-piperidin-3-yl-10H-phenothiazine (3.98 g, 100%) as an off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06992082B2 |
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| Source dataset | uspto-grants-2006_01 |
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| ORD ID | ord-a87b607203a64168b3ddc3ce56c44211 |
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| Source note | uspto-grants-2006_01 |
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