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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1836616Generated: October 29, 2026

Dimethylamine → HCID 23518920, compound

https://huagongshe.com/reaction/1836616

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 11559623HCID 11559623—
SolventEthanolHCID 702—
ProductHCID 23518920HCID 23518920—

Reaction Steps

A mixture of the crude cis-2-[5-Cyano-1-(p-toluenesulfonyl)indol-3-yl]cyclopropanecarboxaldehyde, dimethylamine (0.35 ml, 0.7 mmol, 2.0 M/THF), and anhydrous ethanol (10 ml) was heated with stirring until all solids were dissolved. The reaction vessel was removed from the heating source and sodium triacetoxyborohydride (300 mg, 1.41 mmol) was added. After stirring for 1 h, the solvent was evaporated. The residue was taken up in brine (10 ml) and aqueous 1N sodium hydroxide was added until solids disappeared. The aqueous layer was extracted with ethyl acetate ((4×10 ml), dried over anhydrous magnesium sulfate, and concentrated in vacuo to give the crude cis-2-[5-cyano-1-(p-toluenesulfonyl)indol-3-yl]-1-(N,N-dimethylaminomethyl)cyclopropane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06777437B2
Source datasetuspto-grants-2004_08
ORD IDord-8f44de28aa1b47adbacbdc47367197aa
Source noteuspto-grants-2004_08