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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1508288Generated: October 29, 2026

Aniline → Hydrochloric Acid

https://huagongshe.com/reaction/1508288

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantTrifluoroacetic acidHCID 6422—
ReactantBenzoyl chlorideHCID 7412—
Reactant3-Bromobenzyl bromideHCID 69979—
ReactantHCID 89978469HCID 89978469—
ProductHydrochloric AcidHCID 313—
ProductHCID 89978469HCID 89978469—

Reaction Steps

In a similar manner N-(3-((((4R,4aS,6R,7R,7aR,12bS)-3-(cyclopropylmethyl)-9-hydroxy-7-methoxy-1,2,3,4,5,6,7,7a-octahydro-4a,7-ethano-4,12-methanobenzofuro[3,2-e]isoquinolin-6-yl)methoxy)methyl)phenyl)benzamide (Compound 74) was prepared from C using 3-bromobenzyl bromide, followed by conversion of the aryl bromide to the aniline, subsequent reaction of the aniline with benzoyl chloride and final cleavage of the p-methoxybenzyl group by TFA. Purification by flash column chromatography (silica gel, 0-10% MeOH/DCM) followed by HCl salt formation gave Compound 74 HCl salt as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221831B2
Source datasetuspto-grants-2015_12
ORD IDord-98f8e212eb434c7e95421c2e65cd4a07
Source noteuspto-grants-2015_12