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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1269814Generated: October 31, 2026

Acetic Acid → HCID 178484114, compound

https://huagongshe.com/reaction/1269814

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantFormaldehydeHCID 712—
ReactantSodium HydroxideHCID 14798—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantEther hydrochlorideHCID 10953452—
ReactantHCID 178511699HCID 178511699—
SolventMethanolHCID 887—
ProductHCID 178484114HCID 17848411486%

Reaction Steps

Acetic acid (0.05 ml, 0.87 mmol) was added to a solution of the trans-4-(1H-indazol-5-yloxy)cyclohexanamine (0.044 g, 0.19 mmol) obtained in Example 384 and paraformaldehyde (0.040 g, 1.33 mmol) in methanol (4 ml), and the resulting mixture was stirred for 15 minutes and then ice-cooled. Sodium cyanoborohydride (0.055 g, 0.87 mmol) was added thereto and the resulting mixture was slowly warmed up to room temperature and stirred overnight. After a 1N-aqueous sodium hydroxide solution was added thereto, the solvent was distilled off under reduced pressure and the residue was dried up and then purified by a silica gel chromatography (eluent: chloroform/methanol/30%-aqueous ammonia=300/10/3). A solution of the purified residue in ethyl acetate was prepared, followed by adding thereto a 1N-hydrochloric acid-diethyl ether solution (0.5 ml). The solid precipitated was subjected to decantation with ethyl acetate (three times) and then dried up to obtain trans-4-(1H-indazol-5-yloxy)-N,N-dimethylcyclohexanamine monohydrochloride (0.0400 g, 86%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07199147B2
Source datasetuspto-grants-2007_04
ORD IDord-635b7b80c8e3470eab563865116beb36
Source noteuspto-grants-2007_04