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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1891884Generated: October 31, 2026

Sodium Chloride → (6-Amino-5-ethynyl-pyridin-2-yl)-methanol

https://huagongshe.com/reaction/1891884

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantPotassium CarbonateHCID 11430—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-Amino-6-hydroxymethyl-pyridine-3-carbaldehydeHCID 59255500—
Reactant(1E)-1-diazo-1-dimethoxyphosphorylpropan-2-oneHCID 136023029—
SolventMethanolHCID 887—
Product(6-Amino-5-ethynyl-pyridin-2-yl)-methanolHCID 5528594079.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a mixture of 2-amino-6-hydroxymethyl-pyridine-3-carbaldehyde (16 mg, 0.11 mmol) described in Manufacturing Example 169-1-1 and methanol (1.5 mL) were added dimethyl (1-diazo-2-oxopropyl)phosphonate (30 mg, 0.16 mmol) and potassium carbonate (23 mg, 0.17 mmol) at −10° C., which was stirred for 10 minutes at 0° C., and then for another 6 hours at room temperature. A saturated ammonium chloride aqueous solution and saturated aqueous sodium chloride were added to the reaction mixture at the same temperature, which was extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride, and was concentrated under a reduced pressure. The residue thus obtained was purified by silica gel column chromatography (ethyl acetate) to obtain the title compound (13 mg, 47%, purity: 57%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507530B2
Source datasetuspto-grants-2013_08
ORD IDord-a085d65b8ef944b8a08e7056057a18c4
Source noteuspto-grants-2013_08