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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1400806Generated: November 4, 2026

Potassium tert-butoxide → HCID 67443434, compound

https://huagongshe.com/reaction/1400806

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium tert-butoxideHCID 23665647—
Reactant6-Aminopyridin-3-ol--hydrogen chloride (1/1)HCID 45790888—
Reactanttert-Butyl ((6-(7-chlorothieno[3,2-b]pyridin-2-yl)pyridin-3-yl)methyl)(2-methoxyethyl)carbamateHCID 57919613—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 67443434HCID 6744343454.3%

Reaction Conditions

Temperature95 °C

Reaction Steps

A stirred suspension of 22 (1.0 g, 2.3 mmol), 2-amino-5-hydroxypyridine hydrochloride (405 mg, 2.77 mmol) and potassium tert-butoxide (817 mg, 6.91 mmol) in DMSO (20 mL) under nitrogen was heated to 95° C. for 1 hr then cooled to RT. The reaction mixture was then partitioned between water and AcOEt. The organic layer was successively washed with water, 0.1 N NaOH, a saturated aqueous solution of sodium bicarbonate, a saturated aqueous solution of ammonium chloride and brine, dried over anhydrous magnesium sulfate, filtered and concentrated. The residue was purified twice by Biotage (SNAP 50 g cartridge; MeOH/DCM: 0/100 to 10/90 over 20 CV and Silia Flash 80 g; MeOH/DCM: 0/100 to 10/90 over 20 CV), to afford the title compound 27 (634 mg, 1.249 mmol, 54% yield) as pale yellow sticky oil. MS (m/z): 508.6 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906852B2
Source datasetuspto-grants-2014_12
ORD IDord-e2455d4e02514203850bbc41039255c4
Source noteuspto-grants-2014_12