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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 503883Generated: October 27, 2026

Acetic Anhydride → (3-Amidino-pyrazolo[3,4-b]pyridin-1-yl)-acetic acid tert-butyl ester

https://huagongshe.com/reaction/503883

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 178451226HCID 178451226—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
Product(3-Amidino-pyrazolo[3,4-b]pyridin-1-yl)-acetic acid tert-butyl esterHCID 67103921—

Reaction Steps

[3-(N-Hydroxycarbamimidoyl)-pyrazolo[3,4-b]pyridin-1-yl]-acetic acid tert-butyl ester (6.17 g) in a 100 mL vial was charged with AcOH (45 mL) and Ac2O (4.3 mL). The resultant mixture was stirred at room temperature for 1 h at this time the initial suspension became a clear solution. To this solution was added Pd/C (10%, 900 Mg) and stirred under 1 atm H2 balloon, and resultant mixture was stirred over night at room temperature. Filtration from celite washed with DCM/MeOH and evaporation gave (3-amidino-pyrazolo[3,4-b]pyridin-1-yl)-acetic acid tert-butyl ester which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07777035B2
Source datasetuspto-grants-2010_08
ORD IDord-929dcd9b17be423c851c5201e0b4e968
Source noteuspto-grants-2010_08