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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1934628Generated: October 31, 2026

Hydrochloric Acid → HCID 22467265, compound

https://huagongshe.com/reaction/1934628

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 22467205HCID 22467205—
SolventEthanolHCID 702—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 22467265HCID 2246726579.2%

Reaction Steps

Sodium borohydride (9 mg) was added to a suspension of 6-formyl-3-{1-(7-methoxy-1,3-benzodioxol-5-yl)-2-[(2-methoxy-4-methylphenyl)sulfonamido]-2-oxoethyl}-1-methyl-1H-indole (from Example 96, 130 mg, 0.24 mmol) in a mixture of ethanol (3 ml) and 1,4-dioxane (3 ml) at ambient temperature. Stirring was continued for 1.5 hours, and then water was added dropwise until a solution was achieved. After carefully acidifying with drops of concentrated hydrochloric acid, the solvents were evaporated in vacuo. The residue was partitioned between ethyl acetate and water, and the organic layer was separated and rewashed with water. The organic layer was dried (magnesium sulphate) and the solvents removed in vacuo. The residue was crystallised from a mixture of methanol and diethyl ether to give the title compound (105 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06384070B2
Source datasetuspto-grants-2002_05
ORD IDord-842aee97f86e4e1a8049ae1244bc3aee
Source noteuspto-grants-2002_05