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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1431010Generated: November 1, 2026

Triethylamine → HCID 58528917, compound

https://huagongshe.com/reaction/1431010

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHCID 58528857HCID 58528857—
ReactantHCID 178480602HCID 178480602—
SolventAcetonitrileHCID 6342—
ProductHCID 58528917HCID 5852891772%

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixture of N-(5-bromo-pyridin-2-yl)-4,5-difluoro-2-nitro-benzamide (236 mg, 0.66 mmol), 2-mercapto-1-methylimidazole (83 mg, 0.73 mmol) and triethylamine (0.18 mL, 1.32 mmol) in 2 mL CH3CN was microwave heated to 130° C. for 10 min and the resulting solid was collected by filtration, rinsed with CH3CN, and dried under high vacuum to provide 214 mg (72%) of the title compound as a yellow solid. 1H NMR (500 MHz, DMSO-d6): δ 3.70 (s, 3H), 6.91 (d, 1H, J=7 Hz), 7.20 (d, 1H, J=1 Hz), 7.58 (d, 1H, J=1 Hz), 8.07 (br s, 2H), 8.24 (d, 1H, J=10 Hz), 8.47 (br s, 1H), 11.39 (s, 1H); LCMS (m/z): 452/454 [C16H11BrFN5O3S+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940927B2
Source datasetuspto-grants-2015_01
ORD IDord-125ac07fc72c4867a903888df74d9645
Source noteuspto-grants-2015_01