HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2376993Generated: October 30, 2026
HCID 21099386, compound → HCID 21099380, compound
https://huagongshe.com/reaction/2376993
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 21099386 | HCID 21099386 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21099380 | HCID 21099380 | 78.6% |
Reaction Steps
A stirred THF (1 mL) solution of 1-[2-({4-[(E)-2-(2,4-difluorophenyl)vinyl]phenyl}sulfonyl)phenyl]ethanone (Example 141; 65 mg, 0.17 mmol) was treated with methyl magnesium bromide (3 N in Et2O; 0.17 mL, 0.51 mmol) at ambient temperature. After 75 minutes, the mixture was partitioned between water (20 mL) and EtOAc (20 mL). The phases were separated and the organic phase dried (MgSO4), filtered and concentrated in vacuo. The crude material was purified by flash chromatography on silica (eluant 35% EtOAc/isohexane). The material thus obtained was washed with hexane to afford the title compound as a white solid (53 mg). δH (500 MHz, d6 DMSO): 8.25 (1H, d, J 8.1), 7.71-7.64 (8H, m), 7.53 (1H, t, J 6.1), 7.40 (1H, d, J 16.4), 7.30-7.22 (3H, m), 4.98 (1H, s), 1.56 (6H, s). m/z (ES+) 419 [(M+Na)+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07468393B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-c152abe13eaa4bf8ad1cd32d39cec338 |
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| Source note | uspto-grants-2008_12 |
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