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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1159835Generated: November 2, 2026

HCID 68714375, compound → HCID 86618263, compound

https://huagongshe.com/reaction/1159835

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 68714375HCID 68714375—
CatalystManganese dioxideHCID 14801—
SolventDichloromethane methanolHCID 21226129—
ProductHCID 86618263HCID 8661826326.3%

Reaction Steps

A solution of 6-fluoro-1-(phenylsulfonyl)-1H-indol-5-ol (200 mg, 687 μmol; Intermediate 95) in MeOH (2.14 mL) was treated with 2M NaOH (860 μL) and formaldehyde (2 mL of a 37 wt. % solution in H2O, 26.8 mmol) and heated in an Emrys optimizer (MW) at 120° C. for 5 min. The solvent was removed in vacuo, the residue taken up with H2O and 1M HCl (pH 1), extracted with EtOAc (3×), washed with sat. NaHCO3, brine, dried (Na2SO4) and the solvent removed in vacuo to yield a brownish syrup (265 mg), which was directly used in the oxidation step. A solution of crude 6-fluoro-4-(hydroxymethyl)-1-(phenylsulfonyl)-1H-indol-5-ol (858 μmol) in CH2Cl2/MeOH (4.5+0.1 mL) was treated with MnO2 (1.12 g, 12.9 mmol) and stirred at rt for 30 min. The reaction mixture was filtrated over a plug of SiO2 and it was washed with CH2Cl2 (40 mL) to give the title compound as yellow solid (72 mg). This material was directly used in the next steps.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07812017B2
Source datasetuspto-grants-2010_10
ORD IDord-836dedb388a84289859611cba2b23c00
Source noteuspto-grants-2010_10