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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2046738Generated: November 2, 2026

Sodium Hydroxide → HCID 66932435, compound

https://huagongshe.com/reaction/2046738

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant5-FluoroindoleHCID 67861—
Reactant(E)-3-{1'-tert-butoxycarbonyl-4-oxo-spiro[chromane-2,4'-piperidine]-6-yl}-acrylic acid methyl esterHCID 52952087—
ProductHCID 66932435HCID 6693243563%

Reaction Steps

(E)-3-{1′-(5-Fluoro-1H-indol-3-ylmethyl)-4-oxo-spiro[chromane-2,4′-piperidine]-6-yl}-acrylic acid methyl ester was obtained starting from (E)-3-{4-oxo-spiro[chromane-2,4′-piperidine]-6-yl}-acrylic acid methyl ester (135 mg, 0.45 mmol, Intermediate 1, free base) and 5-fluoro-1H-indole, according to the procedure described in Example 50, Step A (170 mg, 85%). The methyl ester was hydrolyzed with 4 M NaOH following the procedure described in Example 40, Step B, giving (E)-3-{1′-(5-fluoro-1H-indol-3-ylmethyl)-4-oxo-spiro[chromane-2,4′-piperidine]-6-yl}-acrylic acid (100 mg, 63%). The resulting product was treated with NH2OTHP according to the procedure described in Example 40, Step C, giving (E)-3-{1′-(5-fluoro-1H-indol-3-ylmethyl)-4-oxo-spiro[chromane-2,4′-piperidine]-6-yl}-N-(tetrahydro-pyran-2-yloxy)-acrylamide. Finally, removal of the THP protecting group following the procedure described in Example 40, Step C gave (E)-3-{1′-(5-fluoro-1H-indol-3-ylmethyl)-4-oxo-spiro[chromane-2,4′-piperidine]-6-yl}-N-hydroxy-acrylamide hydrochloride (76 mg) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592444B2
Source datasetuspto-grants-2013_11
ORD IDord-784257b837fe46a2aa8258d6666fbe37
Source noteuspto-grants-2013_11