HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844562Generated: October 29, 2026
HCID 86720685, compound → HCID 71187175, compound
https://huagongshe.com/reaction/1844562
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 86720685 | HCID 86720685 | — |
| Reactant | HCID 178418443 | HCID 178418443 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 71187175 | HCID 71187175 | — |
Reaction Steps
Ethyl magnesium bromide (0.53 g, 3.96 ml, 3.98 mmol) was added drop wise to a solution of 5-(4′-(N-((dimethylamino)methylene)sulfamoyl)-6-methoxy-[1,1′-biphenyl]-3-yl)-N-methoxy-N,1,4-trimethyl-1H-pyrrole-2-carboxamide (Step 5, 0.4 g, 0.80 mmol) in anhydrous THF (10 ml) under stirring at 25° C. The reaction mixture was heated at 70-75° C. for 1 hour. The progress of the reaction was monitored by TLC. The reaction mixture was then cooled to 0° C. and was quenched by addition of saturated solution of ammonium chloride (10 ml). The resulting mixture was extracted with ethyl acetate (3×30 ml). The combined organic layer was dried over anhydrous Na2SO4. The solvent was evaporated from the dried organic layer under reduced pressure to obtain a crude product, which was then purified by column chromatography using mixture of ethyl acetate and hexane as an eluent to obtain the title compound 10 (0.04 g, 12.12%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08946432B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-ea175d5d388048309a4a8effdd9abe5c |
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| Source note | uspto-grants-2015_02 |
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