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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1878312Generated: November 2, 2026

Diisopropyl diazene-1,2-dicarboxylate → tert-Butyl 3-(2-(3-(5-bromopyrazin-2-ylamino)-1H-pyrazol-5-yl)-3-methoxyphenoxy)propylcarbamate

https://huagongshe.com/reaction/1878312

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Reactanttert-butyl N-(3-hydroxypropyl)carbamateHCID 3838134—
Reactant2-(3-(5-Bromopyrazin-2-ylamino)-1H-pyrazol-5-yl)-3-methoxyphenolHCID 136337811—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl 3-(2-(3-(5-bromopyrazin-2-ylamino)-1H-pyrazol-5-yl)-3-methoxyphenoxy)propylcarbamateHCID 8665439154%

Reaction Steps

Diisopropyl azodicarboxylate (1.73 mL, 8.76 mmol) is added to a stirred solution of tert-butyl 3-hydroxypropylcarbamate (0.83 mL, 4.83 mmol), 2-(3-(5-bromopyrazin-2-ylamino)-1H-pyrazol-5-yl)-3-methoxyphenol) (1.59 g, 4.38 mmol) and polystyrene triphenylphosphine (5.91 g, 8.76 mmol) in THF (50 mL) at room temperature. After stirring for 45 min, the reaction is filtered, and the solvent is removed under reduced pressure. The resulting residue is chromatographed (methanol/CH2Cl2) to afford 1.27 g (54%) of a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314108B2
Source datasetuspto-grants-2012_11
ORD IDord-5f05a11c5db145a0b3799dda02358add
Source noteuspto-grants-2012_11