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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850672Generated: October 30, 2026

Phenylsilane → 2-Amino-6-(cyanomethyl)-pyrazolo[1,5-a]pyrimidine-3-carboxylic acid

https://huagongshe.com/reaction/1850672

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylsilaneHCID 12752—
ReactantAllyl 2-amino-6-(cyanomethyl)-pyrazolo[1,5-a]pyrimidine-3-carboxylateHCID 86720890—
CatalystHCID 178418397HCID 178418397—
SolventDichloromethaneHCID 6344—
Product2-Amino-6-(cyanomethyl)-pyrazolo[1,5-a]pyrimidine-3-carboxylic acidHCID 86720892100%

Reaction Steps

To a suspension of allyl 2-amino-6-(cyanomethyl)-pyrazolo[1,5-a]pyrimidine-3-carboxylate 4c (10.2 g, 39.65 mmol) in DCM (350 mL) was added phenylsilane (8.581 g, 9.773 mL, 79.3 mmol), followed by Pd(PPh3)4 (1.5 g, 1.298 mmol). The reaction was stirred at room temperature for 2 h. The reaction mixture was filtered and the solid was washed with DCM and dried under vacuum to provide 2-amino-6-(cyanomethyl)-pyrazolo[1,5-a]pyrimidine-3-carboxylic acid 5c as a yellow solid (8.61 g, 100% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957078B2
Source datasetuspto-grants-2015_02
ORD IDord-a4d92c5750984541a2cd8f116d8359ef
Source noteuspto-grants-2015_02