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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1832099Generated: October 30, 2026

Triethylamine → HCID 22051000, compound

https://huagongshe.com/reaction/1832099

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 22050409HCID 22050409—
SolventAcetonitrileHCID 6342—
ProductHCID 22051000HCID 2205100059.5%

Reaction Steps

To a suspension of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-({5-[(methylamino)methyl]pyrazin-2-yl}methyl)pyridin-2(1H)-one (0.16 g, 0.34 mmol) in acetonitrile at 0° C. was added triethylamine (0.043 g, 0.42 mmol), followed by the addition of methane sulfonylchloride (0.047 g, 0.41 mmol) and stirred at room temperature for 1 h under argon atmosphere. The solvents were removed in vacuo and the residue was triturated with water and filtered. It was washed with water an, acetonitrile and dried in vacuo to afford 0.11 g of material. 1H NMR (CD3OD/400 MHz) δ 8.62 (s, 1H), 8.55 (s, 1H), 7.61 (m, 1H), 7.0 (m, 2H), 6.53 (s, 1H), 5.47 (s, 2H), 5.29 (s, 2H), 4.49 (s, 2H), 2.95 (s, 3H), 2.85 (s, 3H), and 2.55 (s, 3H); 19F NMR (CD3OD/400 MHz) −111.70 (m) and −116.07 (m); ES-HRMS m/z 543.0515 (M+H calcd for C21H22BrF2N4O4S requires 543.0508).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07067540B2
Source datasetuspto-grants-2006_06
ORD IDord-714d19e3f6fb497d8b631fe3250d9c12
Source noteuspto-grants-2006_06