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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2173758Generated: October 30, 2026

Acetic Acid → Methyl 3-[2-(2,6-bis-hydroxymethyl-pyridin-4-yloxy)-ethylamino]-propanoate

https://huagongshe.com/reaction/2173758

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantTrifluoroacetic acidHCID 6422—
ReactantTrimethylsilyldiazomethaneHCID 167693—
ReactantTert-butyl 3-[2-(2,6-bis-hydroxymethyl-pyridin-4-yloxy)-ethylamino]-propanoateHCID 66716290—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
ProductMethyl 3-[2-(2,6-bis-hydroxymethyl-pyridin-4-yloxy)-ethylamino]-propanoateHCID 6671416526.6%

Reaction Steps

To a solution of 670 mg of tert-butyl 3-[2-(2,6-bis-hydroxymethyl-pyridin-4-yloxy)-ethylamino]-propanoate in 20 ml of DCM was added 2 ml of TFA. The mixture was stirred for 6 hours at room temperature and then concentrated under reduced pressure, taken up in DCM and concentrated again under reduced pressure. To the residue obtained, dissolved in 10 ml of MeOH, was added, at 5° C., 7 ml of a 2M solution of (trimethylsilyl)diazomethane in hexane. The mixture was stirred for 1 hour 30 minutes at 5° C. and then 200 μl of acetic acid were added. The mixture was taken up in 30 ml of water and 30 ml of EtOAc. The aqueous phase was extracted 2× with 30 ml of EtOAc. The organic phases were combined, washed with saturated NaCl solution, concentrated under reduced pressure and purified by flash chromatography on silica (Analogix Super Flash SiO2 SF15-24g), using a gradient of 0 to 10% MeOH in DCM. The fractions containing the desired product were combined and concentrated under reduced pressure. 155 mg of methyl 3-[2-(2,6-bis-hydroxymethyl-pyridin-4-yloxy)-ethylamino]-propanoate were obtained. LC/MS (C): tr=2.56 min; [M+H]+: m/z 470.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056914B2
Source datasetuspto-grants-2015_06
ORD IDord-840cb5b71dc34c368aa3a1024273d0b0
Source noteuspto-grants-2015_06