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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 278131Generated: October 31, 2026

Sodium borohydride → HCID 22627373, compound

https://huagongshe.com/reaction/278131

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 22627257HCID 22627257—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22627373HCID 2262737339.8%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of 1-(2-chlorobenzyl)-3-isobutyryl-2-propylindole-6-carbonitrile (70 mg) in a mixture of methanol (2 ml) and tetrahydrofuran (2 ml) was added sodium borohydride (21 mg) at 25° C. After stirred at 25° C. for 2 hours, the reaction mixture was partitioned between ethyl acetate and 1N hydrochloric acid. The organic layer was washed with water and brine, dried over magnesium sulfate, and evaporated in vacuo. The residue was crystallized from diisopropyl ether to give 1-(2-chlorobenzyl)-3-(1-hydroxy-2-methylpropyl)-2-propylindole-6-carbonitrile (28 mg) as pale yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06358992B1
Source datasetuspto-grants-2002_03
ORD IDord-9a5b5f5a8ef943aaab82350bbbdb01b9
Source noteuspto-grants-2002_03