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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 78173Generated: October 27, 2026

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

https://huagongshe.com/reaction/78173

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 numberUS08841327B2
Source datasetuspto-grants-2014_09
ORD IDord-8332705e1d4a430bb2e1c0b6ead30dc1
Source noteuspto-grants-2014_09