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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2211925Generated: November 1, 2026

3-(1-Piperazinyl)-1,2-benzisothiazole monohydrochloride → HCID 21963234, compound

https://huagongshe.com/reaction/2211925

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(1-Piperazinyl)-1,2-benzisothiazole monohydrochlorideHCID 11521711—
ReactantHCID 21963167HCID 21963167—
ProductHCID 21963234HCID 2196323456%

Reaction Steps

Starting with N-[5-(2-chloro-acetyl)-2-isopropyl-phenyl]-acetamide (0.50 g, 1.971 mmol), and 3-piperazin-1-yl-benzo[d]isothiazole hydrochloride (0.504 g, 1.971 mmol) and following the procedure as outlined in Example 517, N-{5-[2-(4-benzo[d]isothiazol-3-yl-piperazin-1-yl)-acetyl]-2-isopropyl-phenyl}-acetamide (0.480 g, 1.099 mmol) was obtained as its hydrochloride salt from treatment with dioxane/HCl(gas). Yield=56%. 100% purity at 254 nM. 1H NMR (400 MHz, DMSO-d6) δ 10.46 (bs, 1H), 9.63 (s, 1H), 8.12 (d, J=8.13 Hz, 1H), 8.09 (d, J=8.13 Hz, 1H), 7.90 (s, 1H), 7.79 (d, J=8.13 Hz, 1H), 7.61–7.52 (m, 2H), 7.45 (t, J=7.47 Hz, 1H), 5.13 (s, 2H), 4.12–4.01 (m, 2H), 3.67–3.49 (m, 8H), 3.40 (bs, H2O), 3.37–3.30 (m, 1H), 3.23 (heptet, J=6.81 Hz, 1H), 2.07 (s, 3H), 1.14 (d, J=6.81 Hz, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07101886B2
Source datasetuspto-grants-2006_09
ORD IDord-6cbe0c2a5b084e3f8b60a1e5b25290b6
Source noteuspto-grants-2006_09