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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 536508Generated: October 29, 2026

Ethanamine, 2,2,2-trifluoro- → 2-[1-(2-Fluorobenzyl)-1,4,5,6-tetrahydrocyclopenta[c]pyrazol-3-yl]-5,5-dimethyl-4-[(2,2,2-trifluoroethyl)amino]-5,7-dihydro-6H-pyrrolo[2,3-d]pyrimidin-6-one

https://huagongshe.com/reaction/536508

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanamine, 2,2,2-trifluoro-HCID 9773—
ReactantHCID 71746453HCID 71746453—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product2-[1-(2-Fluorobenzyl)-1,4,5,6-tetrahydrocyclopenta[c]pyrazol-3-yl]-5,5-dimethyl-4-[(2,2,2-trifluoroethyl)amino]-5,7-dihydro-6H-pyrrolo[2,3-d]pyrimidin-6-oneHCID 71285735—

Reaction Conditions

Temperature170 °C

Reaction Steps

50 mg (0.09 mmol) of 2-[1-(2-fluorobenzyl)-1,4,5,6-tetrahydrocyclopenta[c]pyrazol-3-yl]-4-iodo-5,5-dimethyl-5,7-dihydro-6H-pyrrolo[2,3-d]pyrimidin-6-one (example 33A) was dissolved in 1 ml of absolute NMP and 336 mg (3.70 mmol) of 2,2,2-trifluoroethanamine was added. The mixture was heated in the microwave for 2 h at 150° C., 18 h at 150° C., 2 h at 160° C., 2 h at 170° C. and 5 h at 170° C. The reaction solution was filtered and purified by preparative HPLC (eluent: acetonitrile/water with 0.1% formic acid, gradient 20:80→100:0). 18 mg (purity 88%, 36% of theor.) of the target compound was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859569B2
Source datasetuspto-grants-2014_10
ORD IDord-4f472436d32549a9ba06aecc0c3b76da
Source noteuspto-grants-2014_10