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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 910263Generated: October 28, 2026

Diisopropylethylamine → N-((5-Butyl-1-(5-methyl-4-(thiophen-2-yl)pyrimidin-2-yl)-1H-pyrazol-4-yl)methyl)-1,2-dimethyl-1H-imidazole-5-sulfonamide

https://huagongshe.com/reaction/910263

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1,2-dimethyl-1H-imidazole-5-sulfonyl chlorideHCID 2736258—
Reactant(5-butyl-1-(5-methyl-4-(thiophen-2-yl)pyrimidin-2-yl)-1H-pyrazol-4-yl)methanamineHCID 60207818—
SolventDichloromethaneHCID 6344—
ProductN-((5-Butyl-1-(5-methyl-4-(thiophen-2-yl)pyrimidin-2-yl)-1H-pyrazol-4-yl)methyl)-1,2-dimethyl-1H-imidazole-5-sulfonamideHCID 60207824—

Reaction Steps

The title compound was prepared by mixing a sample of (5-butyl-1-(5-methyl-4-(thiophen-2-yl)pyrimidin-2-yl)-1H-pyrazol-4-yl)methanamine, (from Step 3 of Example 36), 1,2-dimethyl-1H-imidazole-5-sulfonyl chloride and diisopropylethylamine in dichloromethane. 1H NMR (400 MHz, CD3OD) δ 8.68 (s 1H), 7.94 (m, 1H), 7.78 (m, 1H), 7.56 (m, 1H), 7.37 (m, 1H), 7.29 (m, 1H), 4.09 (s 2H), 3.70 (s 3H), 3.18 (br t, 2H), 2.64 (s, 3H), 2.35 (s, 3H), 1.49 (m, 2H), 1.32 (m, 2H), 0.84 (m 3H). LCMS (ES+) m/z 486 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022061B2
Source datasetuspto-grants-2011_09
ORD IDord-6fa50c23e1c243999b8647c07ca75cd8
Source noteuspto-grants-2011_09