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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1191902Generated: October 30, 2026

Hydrochloric Acid → HCID 58173248, compound

https://huagongshe.com/reaction/1191902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86651735HCID 86651735—
SolventMeOH tetrahydrofuranHCID 21899815—
ProductHCID 58173248HCID 58173248—

Reaction Steps

To the solution of 1-(4-chloro-3-nitro-benzenesulfonyl)-5-methyl-1H-indole-3-carbaldehyde (284.10 mg, 0.75 mmol) in the mixture of methanol/THF (1:1, 20 mL), NaBH4(32 mg, 0.825 mmol) was added slowly at 0° C. After addition, the reaction was stirred for additional 30 min at same temperature. 1.0 ml of 1N HCl was added after reaction was completed, as determined by checking using thin layer chromatography (TLC). The resulting reaction mixture was concentrated, and the residue was diluted with water (20 ml) and extracted with ethyl acetate (3×10 ml). The combined organic layers was washed with water, 10% NaHCO3, and brine, dried with MgSO4, filtered and concentrated. The residue was purified with column chromatography to give pure product, OSU-A9M (248.5 mg, 87%) as off white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680133B2
Source datasetuspto-grants-2014_03
ORD IDord-12e7503f106a4489bacb623c229b6f3d
Source noteuspto-grants-2014_03