Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantN,N-DimethylanilineHCID 949—
ReactantPiperazineHCID 4837—
ReactantPhosphorus oxychlorideHCID 24813—
Reactant8-chlorodibenzo[b,f][1,4]thiazepin-11(10H)-oneHCID 827105—
SolventTolueneHCID 1140—
Product8-Chloro-11-(piperazin-1-yl)-dibenzo[b,f][1,4]thiazepineHCID 1135942313.3%

Reaction Conditions

Temperature100 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07622461B2
Source datasetuspto-grants-2009_11
ORD IDord-5ae6b28ad035493f857cdca8759b4349
Source noteuspto-grants-2009_11