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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2211917Generated: October 25, 2026

N-[4-(2-chloro-ethyl)-2-methyl-phenyl]-N-propyl-acetamide → N-(4-{2-[4-(1H-Indazol-3-YL)-piperazin-1-YL]-ethyl}-2-methyl-phenyl)-N-propyl-acetamide hydrochloride

https://huagongshe.com/reaction/2211917

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-[4-(2-chloro-ethyl)-2-methyl-phenyl]-N-propyl-acetamideHCID 21963280—
Reactant3-(Piperazin-1-yl)-1H-indazole hydrochlorideHCID 21963434—
ProductN-(4-{2-[4-(1H-Indazol-3-YL)-piperazin-1-YL]-ethyl}-2-methyl-phenyl)-N-propyl-acetamide hydrochlorideHCID 2196355620%

Reaction Steps

N-[4-(2-Chloro-ethyl)-2-methyl-phenyl]-N-propyl-acetamide (0.090 g, 0.355 mmole) was reacted with 3-piperazin-1-yl-1H-indazole hydrochloride (0.127 g, 0.532 mmol) according to the method outlined in Example 501. The titled product was precipitated as its hydrochloride salt from dioxane/HCl(gas) treatment (0.030 g, 0.071 mmol). Yield=20%. 100% purity at 254 nm; LCMS (APCI): 437.3 [M+H]+, 1H NMR (400 MHz, DMSO-d6) δ 12.19 (s, 1H), 10.50 (s, 1H), 7.79 (d, J=8.55 Hz, 1H), 7.37 (d, J=8.55 Hz, 1H), 7.32–7.26 (m, 2H), 7.21–7.12 (m, 2H), 6.99 (t, J=7.48 Hz, 1H), 3.97 (bd, J=8.70 Hz, 2H), 3.87–3.77 (m, 1H), 3.65 (bd, J=7.25 Hz, 2H), 3.39 (bs, DMSO-H2O), 3.31–3.21 (m, 6H), 3.10–2.92 (m, 3H), 2.14 (s, 3H), 1.58 (s, 3H), 1.39 (sextet, J=7.38 Hz, 2H), 0.79 (t, 7.38 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07101886B2
Source datasetuspto-grants-2006_09
ORD IDord-55e4b1c3170640c6a5ce1c2e7a658f31
Source noteuspto-grants-2006_09