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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1241638Generated: October 31, 2026

Sodium Hydroxide → tert-Butyl 5-(hydroxymethyl)pyridin-2-ylcarbamate

https://huagongshe.com/reaction/1241638

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantEthyl 6-(((tert-butoxy)carbonyl)amino)pyridine-3-carboxylateHCID 21879719—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl 5-(hydroxymethyl)pyridin-2-ylcarbamateHCID 357538989.2%

Reaction Steps

To 4.6 mL (4.6 mmol) of a 1M solution of lithium aluminum hydride in diethyl ether at −40 C under a nitrogen atmosphere, was added a slution of 618 mg (2.3 mmol) of ethyl 6-(tert-butyloxycarbonylamino)nicotinate from part B in 40 mL of anhydrous tetrahydrofuran. After the addition, this was warmed to room temperature, stirred for 3 hours, cooled to 0 C, and 145 μL of water, 145 μL of 20% sodium hydroxide solution and 290 μL of water were successively added. To the resulting mixture was added 50 mL of tetrahydrofuran and stirring continued for 30 minutes. Anhydrous magnesium sulfate was added, the solids removed via filtration and the filtrate concentrated under reduced pressure to afford 460 mg of the desired product, m/e=224(M+), which was used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115618B2
Source datasetuspto-grants-2006_10
ORD IDord-30ea744e74e045b69c5d42f1a6a645be
Source noteuspto-grants-2006_10