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5-chloro-3-ethynylpyridin-2-amine synthesis

4synthesis methods
866318-90-3 Synthesis
2-AMINO-5-CHLORO-3-(TRIMETHYLSILYL)ACETYLENYLPYRIDINE

866318-90-3
27 suppliers
$45.00/10mg

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Yield:866318-88-9 92%

Reaction Conditions:

Stage #1: 2-amino-5-chloro-3-[(trimethylsilyl)ethynyl]pyridinewith potassium tert-butylate in ethanol at 20 - 30;
Stage #2: with acetic acid in water;

Steps:

7.2 Step two:

Dissolve potassium tert-butoxide (0.2g) in ethanol (20.0g), control the temperature at 20-30°C, add compound 6 (20.0g) in batches, and keep the reaction until HPLC detects the raw material (compound 2). Less than 0.5%, add acetic acid (0.2g) and water (60.0g), filter and dryCompound 7 (12.5 g, yield 92.0%) was obtained.

References:

CN112574218,2021,A Location in patent:Paragraph 0124; 0129-0131