HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1437019Generated: October 25, 2026
Hydrochloric Acid → 8-Chloro-11-(piperazin-1-yl)-dibenzo[b,f][1,4]thiazepine
https://huagongshe.com/reaction/1437019
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | N,N-Dimethylaniline | HCID 949 | — |
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 8-chlorodibenzo[b,f][1,4]thiazepin-11(10H)-one | HCID 827105 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 8-Chloro-11-(piperazin-1-yl)-dibenzo[b,f][1,4]thiazepine | HCID 11359423 | 13.3% |
Reaction Steps
To a mixture of 8-chloro-10H-dibenzo[b,f][1,4]thiazepin-11-one (189JO13) (38 mg, 0.15 mmol) and N,N-dimethylaniline (46 μL, 0.36 mmol) in toluene was added POCl3 (27 μL, 0.29 mmol) and the resulting mixture was stirred for 2 h at 100° C., and then concentrated. Toluene (2 mL) and piperazine (62 mg, 0.73 mmol) were added, and the resulting mixture was stirred at 100° C. for 3 h, and then allowed to obtain room temperature. To the mixture was added aqueous HCl (1 mL, 2 M) and then the aqueous phase was extracted with EtOAc (2×2 mL). To the aqueous phase was added aqueous NaOH (3 mL, 2 M) and the resulting mixture was extracted with EtOAc (3×3 mL). The combined organic phases were concentrated and purified by HPLC to give 6.6 mg of the title compound (189JO16). MS (ESI) 330 (MH+). Purity for MH+ (UV/MS) 99/98.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07622461B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-5ae6b28ad035493f857cdca8759b4349 |
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| Source note | uspto-grants-2009_11 |
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