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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2211922Generated: October 31, 2026

Methacryloyl chloride → HCID 21963432, compound

https://huagongshe.com/reaction/2211922

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethacryloyl chlorideHCID 13528—
ReactantHCID 21963230HCID 21963230—
ProductHCID 21963432HCID 2196343273%

Reaction Steps

Starting with 4-[2-(4-benzo[d]isothiazol-3-yl-piperazin-1-yl)-ethyl]-2-methyl-phenylamine hydrochloride (0.6 g, 1.702 mmol) and 2-methyl-acryloyl chloride (0.206 mL, 1.702 mmol) and following the procedure outlined in Example 512, N-{4-[2-(4-Benzo[d]isothiazol-3-yl-piperazin-1-yl)-ethyl]-2-methyl-phenyl}-2-methyl-acrylamide (0.521 g, 1.239 mmole) was obtained. Yield=73%. 100% purity at 254 nM; LCMS (APCI): 421.3 [M+H]+; 1H NMR (400 MHz, DMSO-d6) 811.17 (bs, 1H), 9.32 (s, 1H), 8.10 d, J=7.88 Hz, 1H), 8.07 (d, J=7.88 Hz, 1H), 7.55 (t, J=7.88 Hz, 1H), 7.43 (t, J=7.88 Hz, 1H), 7.19 (d, J=7.88 Hz, 1H), 7.11 (s, 1H), 7.05 (d, J=7.88 Hz, 1H), 5.80 (s, 1H), 5.44 (s, 1H), 4.05 (bd, J=12.08 Hz, 2H), 3.63 (bd, J=12.08 Hz, 2H), 3.51–3.32 (m, 5H), 3.31 (s, H2O), 3.29–3.22 (m, 1H), 3.07–2.98 (m, 2H), 2.12 (s, 3H), 1.90 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07101886B2
Source datasetuspto-grants-2006_09
ORD IDord-94f00aa8517b44138ebfaefdd76dff56
Source noteuspto-grants-2006_09