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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1256358Generated: October 30, 2026

N,N-dimethylpiperazine-1-sulfonamide → HCID 67064363, compound

https://huagongshe.com/reaction/1256358

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-dimethylpiperazine-1-sulfonamideHCID 1094966—
ReactantN-(7-chloro-2-methylpyrazolo[1,5-a]pyrimidin-5-yl)-4-(2-hydroxypropan-2-yl)benzamideHCID 86652267—
CatalystDimethyl SulfoxideHCID 679—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
ProductHCID 67064363HCID 6706436381%

Reaction Steps

A solution of N-(7-chloro-2-methylpyrazolo[1,5-a]pyrimidin-5-yl)-4-(2-hydroxypropan-2-yl)benzamide (2F, 86 mg, 0.25 mmol) and N,N-dimethylpiperazine-1-sulfonamide (145 mg, 0.75 mmol) in DMF (1.0 mL) was stirred at 100° C. for 2 h. After cooling to room temperature, the mixture was diluted with a few drops of DMSO and methanol, and was then purified by preparatory HPLC (35-60% MeCN/H2O gradient+0.01% TFA). Lyophilization of the combined fractions gave the titled compound as a white solid (101.3 mg, 81%). 1H NMR (DMSO-d6) δ: 10.90 (s, 1H), 8.00 (d, J=8.8 Hz, 2H), 7.60 (d, J=8.6 Hz, 2H), 7.36 (s, 1H), 6.20 (s, 1H), 3.79-3.82 (m, 4H), 3.39-3.48 (m, 4H), 3.07-3.16 (m, 2H), 2.39 (s, 3H), 1.66-1.82 (m, 2H), 1.45 (s, 6H), 1.01 (t, 3H); ESI-MS: m/z 502.3 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461163B2
Source datasetuspto-grants-2013_06
ORD IDord-09f88174fa704ce18dcfc29adb3cbb80
Source noteuspto-grants-2013_06