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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 536522Generated: November 1, 2026

(1-Methyl-1H-pyrazol-5-yl)methanamine → HCID 71285373, compound

https://huagongshe.com/reaction/536522

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(1-Methyl-1H-pyrazol-5-yl)methanamineHCID 7019421—
Reactant2-[1-(2-Fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl]-4-iodo-5,5-dimethyl-5,7-dihydro-6H-pyrrolo[2,3-d]pyrimidin-6-oneHCID 86705367—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 71285373HCID 71285373—

Reaction Steps

111.1 mg (1.0 mmol) of 1-(1-methyl-1H-pyrazol-5-yl)methanamine was put in a vial of a microwave reactor block and a solution of 51.4 mg (100 μmol) of 2-[1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl]-4-iodo-5,5-dimethyl-5,7-dihydro-6H-pyrrolo[2,3-d]pyrimidin-6-one (example 15A) in 0.6 ml of 1-methyl-2-pyrrolidinone was added. Then the reactor block was sealed and was irradiated for 6 h with microwaves, in order to reach and maintain a temperature of the mixture of 170° C. After cooling, it was purified by preparative LC-MS (method 6). The product-containing fractions were concentrated by evaporation by means of a centrifugal dryer under vacuum. The residue of the individual fractions was in each case dissolved in 0.6 ml DMSO and combined. Then the solvent was evaporated completely in the centrifugal dryer. 32.7 mg (61% of theor.) of the target product was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859569B2
Source datasetuspto-grants-2014_10
ORD IDord-57d10c9d7e684d33ae197a28270ce874
Source noteuspto-grants-2014_10