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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1403284Generated: October 25, 2026

Potassium Hydroxide → {5-[hydroxy-(7H-pyrrolo[2,3-d]pyrimidin-5-yl)-methyl]-pyridin-2-yl}-(6-methoxy-pyridin-3-ylmethyl)-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/1403284

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant7H-Pyrrolo(2,3-d)pyrimidineHCID 261591—
ReactantSodium BicarbonateHCID 516892—
Reactant(5-Formyl-pyridin-2-yl)-(6-methoxy-pyridin-3-ylmethyl)-carbamic acid tert-butyl esterHCID 57619225—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
Product{5-[hydroxy-(7H-pyrrolo[2,3-d]pyrimidin-5-yl)-methyl]-pyridin-2-yl}-(6-methoxy-pyridin-3-ylmethyl)-carbamic acid tert-butyl esterHCID 5796319221.7%

Reaction Steps

7H-Pyrrolo[2,3-d]pyrimidine (6, 0.450 g, 3.78 mmol), (5-formyl-pyridin-2-yl)-(6-methoxy-pyridin-3-ylmethyl)-carbamic acid tert-butyl ester (71, 1.43 g, 4.16 mmol), potassium hydroxide (0.689 g, 12.3 mmol) and 6.6 mL methanol were combined in a reaction vessel. The reaction mixture was allowed to stir at room temperature for 36 hours, then concentrated under vacuum to provide a thick brown slurry, which was combined with ethyl acetate and aqueous saturated sodium bicarbonate. The organic layer was dried with sodium sulfate, filtered and the filtrate adsorbed onto silica. This was purified by silica gel column chromatography, eluting with a gradient of 1-10% methanol in dichloromethane over 30 minutes. Appropriate fractions were combined and the solvents removed under vacuum to provide the desired compound (72, 380 mg). 1H NMR was consistent with the compound structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912204B2
Source datasetuspto-grants-2014_12
ORD IDord-4187567eb7d74794b62fd43c24d80752
Source noteuspto-grants-2014_12