HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1845636Generated: November 2, 2026
N-bromobutanimide → methyl 4-(4-bromo-1-methyl-1H-pyrazol-5-yl)-5-ethyl-2-thiophenecarboxylate
https://huagongshe.com/reaction/1845636
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | methyl 5-ethyl-4-(1-methyl-1H-pyrazol-5-yl)-2-thiophenecarboxylate | HCID 57826625 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | methyl 4-(4-bromo-1-methyl-1H-pyrazol-5-yl)-5-ethyl-2-thiophenecarboxylate | HCID 57826735 | — |
Reaction Steps
To a solution of methyl 5-ethyl-4-(1-methyl-1H-pyrazol-5-yl)-2-thiophenecarboxylate (600 mg, 2.40 mmol) [prepared according to Example 98] in Tetrahydrofuran (THF) (10 ml) was added N-bromosuccinimide (512 mg, 2.88 mmol). The mixture stirred in a sealed tube at 70° C. for 2 h. The reaction mixture was then concentrated and purified with silica gel using a 0-5% gradient (ethyl acetate/hexane) to afford the title compound as an off-white solid: LC-MS (ES) m/z 330 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08946278B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-48683c1de63e4bfcb90e3c69ce1eef2a |
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| Source note | uspto-grants-2015_02 |
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