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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2223990Generated: November 1, 2026

HCID 21138071, compound → HCID 59716021, compound

https://huagongshe.com/reaction/2223990

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 21138071HCID 21138071—
SolventAcetonitrileHCID 6342—
ProductHCID 59716021HCID 59716021—

Reaction Steps

4-Methoxybenzyl chloride (15.6 g) was reacted with 2-aminoethanethiol (7.7 g) in methanol and sodium methoxide, to afford of 2-(4-methoxybezyl-sulfanyl)-ethylamine (1) (18.8 g). One half of this material was taken in dichloromethane (cooling bath 0° C.). Chloroacetyl chloride in the same solvent, was added slowly with stirring, followed by an equivalent of triethyl amine to produce 2-chloro N-[2-(4-methoxybenzyl-sulfanyl)-ethyl]acetamide (2) in a 94% yield. Compound 2 was reacted with an equivalent amount of 1 in refluxing acetonitrile for 6 hrs to provide N-[-2-(4-methoxy-benzylsulfanyl)-ethyl]-2-[2-(4-methoxy-benzylsulfanyl)-ethylamino]-acetamide (3) (40.4 g). Compound 3 was reduced with lithium aluminium hydride (LAH) to yield 4 in 85%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07378079B2
Source datasetuspto-grants-2008_05
ORD IDord-02be9a9393304acb80a58d3328d63a72
Source noteuspto-grants-2008_05