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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1171451Generated: November 5, 2026

Borohydride → HCID 11249362, compound

https://huagongshe.com/reaction/1171451

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBorohydrideHCID 28123—
ReactantHCID 58828974HCID 58828974—
ReactantHCID 178481694HCID 178481694—
SolventTetrahydrofuran ethanolHCID 21873804—
ProductHCID 11249362HCID 11249362—

Reaction Steps

265 mg (0.66 mmol, 3 eq) of resin-supported borohydride and 3 mg (0.01 mmol, 0.03 eq) of bis(bipyridine)dibromonickel (II) are added to a solution of 64 mg (0.33 mmol, 1.5 eq) of 4-methyl-5-pyridin-4-yl-4H-[1,2,4]-triazole-3-thiol in 1.5 ml of tetrahydrofuran/ethanol 5/5. To the suspension obtained there is added a solution of 100 mg (0.22 mmol, 1 eq) of ethyl [4-(4-iodo-2-propoxybenzylamino)phenyl]acetate in 1.5 ml of tetrahydrofuran/ethanol 5/5. The reaction mixture is stirred overnight under reflux. After returning to room temperature, the reaction medium is filtered and then concentrated. 0.111 g (97%) of the expected compound is recovered.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829588B2
Source datasetuspto-grants-2010_11
ORD IDord-c1fc7246c9064569a3fa767d778b34f0
Source noteuspto-grants-2010_11