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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1371616Generated: November 1, 2026

Trifluoroacetic acid → Trifluoroacetic acid

https://huagongshe.com/reaction/1371616

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 58777573HCID 58777573—
SolventDichloromethaneHCID 6344—
ProductTrifluoroacetic acidHCID 6422—
Product[4-Amino-2-(piperidin-3-ylamino)-pyrimidin-5-yl]-(2-methoxy-phenyl)-methanoneHCID 21070618—

Reaction Conditions

Temperature0 °C

Reaction Steps

3-[4-Amino-5-(2-methoxy-benzoyl)-pyrimidin-2-ylamino]-piperidine-1-carboxylic acid tert-butyl ester (76 mg, Example 52) was dissolved in dichloromethane (4 mL), cooled to 0° C. and treated with trifluoroacetic acid (1 mL). After stirred 30 minutes at 0° C., the reaction mixture was concentrated in vacuo to give [4-amino-2-(piperidin-3-ylamino)-pyrimidin-5-yl]-(2-methoxy-phenyl)-methanone as a trifluoroacetic acid salt. A portion of this material was partitioned between ethyl acetate and aqueous sodium carbonate to give the free base. (129.5 mg). MS (M+H)+, 328.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157455B2
Source datasetuspto-grants-2007_01
ORD IDord-7092b255de624db19a69b1fd1d3c3b3a
Source noteuspto-grants-2007_01