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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 409121Generated: October 25, 2026

Diisopropyl azodicarboxylate → tert-butyl (2S)-2-([4-amino-3-iodo-1H-pyrazolo[3,4-d]-pyrimidin-1-yl]methyl)-4,4-difluoropyrrolidine-1-carboxylate

https://huagongshe.com/reaction/409121

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropyl azodicarboxylateHCID 5363146—
Reactanttert-Butyl (2S)-4,4-difluoro-2-(hydroxymethyl)pyrrolidine-1-carboxylateHCID 20648576—
ReactantHCID 178508725HCID 178508725—
SolventTetrahydrofuranHCID 8028—
Producttert-butyl (2S)-2-([4-amino-3-iodo-1H-pyrazolo[3,4-d]-pyrimidin-1-yl]methyl)-4,4-difluoropyrrolidine-1-carboxylateHCID 8671450720.8%

Reaction Steps

Under nitrogen, to a solution of 3-iodo-1H-pyrazolo[3,4-d]pyrimidin-4-amine (2.61 g, 10.00 mmol, 1.00 equiv), tert-butyl (2S)-4,4-difluoro-2-(hydroxymethyl)pyrrolidine-1-carboxylate (2.37 g, 9.99 mmol, 1.00 equiv) and TPP (4 g, 15.2 mmol, 1.50 equiv) in THF was DIAD (3.00 g, 15.0 mmol, 1.50 equiv) at 0° C. in 30 min. The resulting solution was stirred overnight at room temperature. The mixture was then concentrated under vacuum and the residue was applied onto a silica gel column with dichloromethane/ethyl acetate (3/1) to give 1 g of tert-butyl (2S)-2-([4-amino-3-iodo-1H-pyrazolo[3,4-d]-pyrimidin-1-yl]methyl)-4,4-difluoropyrrolidine-1-carboxylate as reddish oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759358B1
Source datasetuspto-grants-2014_06
ORD IDord-837b2a2a12d94a1494e7ddc4e51bd917
Source noteuspto-grants-2014_06