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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1726055Generated: November 1, 2026

Ammonium formate → HCID 68840193, compound

https://huagongshe.com/reaction/1726055

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
ReactantHCID 68843999HCID 68843999—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 68840193HCID 68840193104.6%

Reaction Steps

3-(1-tert-Butoxycarbonyl-2,3-dihydro-1H-indol-2-yl)-5-hydroxyindazole-1-carboxylic acid tert-butyl ester is prepared, according to procedure D, using 800 mg of 5-benzyloxy-3-(1-tert-butoxycarbonyl-1H-indol-2-yl)indazole-1-carboxylic acid tert-butyl ester, 560 mg of ammonium formate, and 800 mg of 10% palladium-on-charcoal in 30 ml of absolute ethanol. 700 mg of 3-(1-tert-butoxycarbonyl-2,3-dihydro-1H-indol-2-yl)-5-hydroxyindazole-1-carboxylic acid tert-butyl ester are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491710B2
Source datasetuspto-grants-2009_02
ORD IDord-ab8aa4d3134a4e94bb17d3fbaac7e771
Source noteuspto-grants-2009_02