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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2211927Generated: November 1, 2026

3-(1-Piperazinyl)-1,2-benzisothiazole monohydrochloride → HCID 21963599, compound

https://huagongshe.com/reaction/2211927

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(1-Piperazinyl)-1,2-benzisothiazole monohydrochlorideHCID 11521711—
ReactantHCID 21963361HCID 21963361—
ProductHCID 21963599HCID 2196359967%

Reaction Steps

Starting with N-[4-(2-chloro-acetyl)-3-isopropyl-phenyl]-acetamide (0.876 g, 3.453 mmol), and 3-piperazin-1-yl-benzo[d]isothiazole hydrochloride (0.883 g, 3.453 mmol) and following the procedure as outlined in Example 517, N-{4-[2-(4-benzo[d]isothiazol-3-yl-piperazin-1-yl)-acetyl]-3-isopropyl-phenyl}-acetamide (0.1.0 g, 2.302 mmol) was obtained as its hydrochloride salt from treatment with dioxane/HCl(gas). Yield=67%. 100% purity at 254 nM. 1H NMR (400 MHz, DMSO-d6) δ 10.44–10.29 (bm, 2H), 8.13 (d, J=8.49 Hz, 1H), 8.09 (d, J=8.49 Hz, 1H), 7.81 (d, J=9.12 Hz, 1H), 7.73–7.68 (m, 2H), 7.57 (t, J=7.49 Hz, 1H), 7.45 (t, J=7.49 Hz, 1H), 5.04 (s, 2H), 4.13–4.02 (m, 2H), 3.76–3.45 (m, 18H, H2O), 2.06 (s, 3H), 1.18 (d, J=6.85 Hz, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07101886B2
Source datasetuspto-grants-2006_09
ORD IDord-ffac0d3a545449beb8df5c568a3cd725
Source noteuspto-grants-2006_09