HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1159867Generated: November 2, 2026
HCID 86618263, compound → HCID 68712999, compound
https://huagongshe.com/reaction/1159867
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 86618263 | HCID 86618263 | — |
| Reactant | HCID 178418689 | HCID 178418689 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Tetrahydrofuran toluene | HCID 22635083 | — |
| Product | HCID 68712999 | HCID 68712999 | — |
Reaction Steps
A solution of crude 6-fluoro-5-hydroxy-1-(phenylsulfonyl)-1H-indole-4-carbaldehyde (86.4 mg, 271 μmol; Intermediate 96) in THF (3 mL) was treated with MeMgBr (774 μL of a 1.4 M solution in Toluene/THF, 4 eq) at rt and stirred for 30 min. After 30 min another 2 eq and after 45 min another 4 eq. of Grignard solution were added and stirring continued for 15 min. The reaction mixture was quenched with sat. NH4Cl, extracted with EtOAc (3×), the combined org. phases washed with brine, dried and the solvent removed in vacuo to give a yellow-brownish solid (95.6 mg). This material was purified by prep. HPLC (15-45% MeCN/50 mM NH4HCO3) to yield the title compound as an yellowish solid (31.8 mg, 11% over 3 steps). MS (ESI+) for C16H14FNO4S m/z 318 (M-OH)+, 358 (M+Na)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07812017B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-f8aab3845d7e4af7a22f0d0052193bd3 |
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| Source note | uspto-grants-2010_10 |
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