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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743353Generated: October 30, 2026

HCID 11011683, compound → HCID 9967388, compound

https://huagongshe.com/reaction/1743353

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 11011683HCID 11011683—
Reactant1-Benzyl-3-iodoindazoleHCID 11067603—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 9967388HCID 996738869%

Reaction Steps

A solution of methyl 5-bromofuranoate (0.75 g, 3.66 mmol), hexamethylditin (1.0 g, 3.05 mmol) and Pd(PPh3)4 (90 mg, 0.078 mmol) in DME (50 mL) was heated to reflux overnight. The initial amber coloured solution became black. The solution was allowed to cool and then filtered and concentrated under reduced pressure. The crude stannane was purified by passage through a plug of silica (1:9 EtOAc:cyclohexane) to give methyl 2-trimethylstannyl-5-furanoate (0.17 g, 19%): 1H-NMR (CDCl3); The low yield of the product may be due to its suspected volatility. Pd(PPh3)4 (9 mg, 0.008 mmol) was added to a solution of 1-benzyl-3-iodo-1H-indazole (0.13 g, 0.39 mmol) and methyl 2-trimethylstannyl-5-furanoate (0.17 g, 0.588 mmol) in DME (20 mL).and the mixture was heated to reflux overnight. The reaction mixture was allowed to cool to rt, filtered and concentrated under reduced pressure. Purification of the residue by chromatography on silica (3:7 EtOAc:cyclohexane) gave the product as a slightly contaminated yellow solid (88.6 mg, 69%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07009056B2
Source datasetuspto-grants-2006_03
ORD IDord-bb5cb2caec4e43edb84c3d7ba6446247
Source noteuspto-grants-2006_03