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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2392024Generated: October 30, 2026

N-bromobutanimide → methyl 4-(4-bromo-1-ethyl-1H-pyrazol-5-yl)-2-thiophenecarboxylate

https://huagongshe.com/reaction/2392024

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactantmethyl 4-(1-ethyl-1H-pyrazol-5-yl)-2-thiophenecarboxylateHCID 67066137—
SolventTetrahydrofuranHCID 8028—
Productmethyl 4-(4-bromo-1-ethyl-1H-pyrazol-5-yl)-2-thiophenecarboxylateHCID 5782683678.5%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of methyl 4-(1-ethyl-1H-pyrazol-5-yl)-2-thiophenecarboxylate (0.45 g, 1.9 mmol) [see example 92(a)] in THF (5 mL) was added NBS (0.33 g, 2.5 mmol). The reaction mixture was heated to 70° C. under nitrogen. After 2 h, the reaction mixture was concentrated under vacuum and purified on silica (EtOAc/hexanes, 10-30%) to afford the title compound (0.47 g, 78%). LC-MS (ES) m/z=316 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273782B2
Source datasetuspto-grants-2012_09
ORD IDord-b30216cc01204715a56c37b5f2642349
Source noteuspto-grants-2012_09