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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1604674Generated: November 1, 2026

HCID 19603776, compound → HCID 19603713, compound

https://huagongshe.com/reaction/1604674

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 19603776HCID 19603776—
SolventDichloromethaneHCID 6344—
ProductHCID 19603713HCID 1960371378.8%

Reaction Steps

5-Benzyloxy-1-{[2-(4-tert-butylthiazol-2-yl)benzofuran-5-yl]methyl}-1H-indazole-3-carboxamide (0.122 g) was added to a solution (1 M) of borontribromide in dichloromethane (0.57 ml) under ice-cooling and then the mixture was stirred at room temperature for 1.5 hours. The mixture was concentrated under reduced pressure and the residue was partitioned between aqueous sodium hydrogen carbonate solution and ethyl acetate. The organic layer was separated, dried over magnesium sulfate and concentrated under reduced pressure to give 1-{[2-(4-tert-butylthiazol-2-yl)benzofuran-5-yl]methyl}-5-hydroxy-1H-indazole-3-carboxamide (0.08 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05994378
Source datasetuspto-grants-1999_11
ORD IDord-a7905e90813244e6ba2dcaa28ab9684f
Source noteuspto-grants-1999_11