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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2404200Generated: November 1, 2026

Diisopropylethylamine → {[6-(4-Tert-butyl-cyclohexyloxy)-8-methyl-naphthalen-2-ylmethyl]-amino}-acetic acid methyl ester

https://huagongshe.com/reaction/2404200

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantGlycine methyl ester hydrochlorideHCID 122755—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant6-(4-Tert-butyl-cyclohexyloxy)-8-methyl-naphthalene-2-carbaldehydeHCID 86668429—
Solvent1,2-DichloroethaneHCID 11—
SolventDichloromethaneHCID 6344—
Product{[6-(4-Tert-butyl-cyclohexyloxy)-8-methyl-naphthalen-2-ylmethyl]-amino}-acetic acid methyl esterHCID 6692655188.9%

Reaction Steps

A solution of 6-(4-tert-butyl-cyclohexyloxy)-8-methyl-naphthalene-2-carbaldehyde (50 mg, 0.15 mmol), glycine methyl ester, hydrochloride (27 mg, 0.22 mmol) and N,N-diisopropylethylamine (DIEA) (34 uL) in 1,2-dichloroethane (2 mL) was stirred for 1 hour at room temperature. Then sodium triacetoxyborohydride (52 mg, 0.25 mmol) was added and stirred for 3 hrs. The reaction was diluted with methylene chloride and washed with saturated sodium bicarbonate aqueous, dried over MgSO4, filtered, and concentrated. The crude was purified via silica gel column chromatography eluted 0-5% MeOH in methylene chloride to give the light brown solid (53 mg, yield: 86%). ESI-MS: 420.30 (M+23)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802659B2
Source datasetuspto-grants-2014_08
ORD IDord-1bcd70ff18454a80990d0f23c39fcf29
Source noteuspto-grants-2014_08