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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289488Generated: October 30, 2026

Trifluoroacetic acid → HCID 18697923, compound

https://huagongshe.com/reaction/2289488

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 18697926HCID 18697926—
SolventDichloromethaneHCID 6344—
ProductHCID 18697923HCID 1869792351.9%

Reaction Steps

A solution of 4-(2-(4-tert-butoxycarbonylpiperazin-1-yl)pyrid-5-yl)-N-(9-ethylcarbazol-3-yl)-2-pyrimidineamine (65 mg, 0.12 mmol) in dichloromethane (2 ml) was treated with trifluoroacetic acid (2 ml). After 2h the mixture was evaporated and the residue reconcentrated five times from dichloromethane then three times from diethyl ether. The residue was subjected to column chromatography (silica, 0.88 ammonia solution-methanol-dichloromethane 1:5:94) to afford the title compound (28 mg) as a pale yellow solid m.p. 131-137°. δH (d6DMSO) 1.31 (3H, t, J 7.1 Hz), 2.80 (4H, m), 3.56 (4H, m), 4.42 (2H, q, J 7.1 Hz), 6.93 (1H, d, J 9.1 Hz), 7.17 (1H, m), 7.25 (1H, d, J 5.3 Hz), 7.43 (1H, m), 7.55 (2H, m), 7.76 (1H, dd, J 2.9, 8.8 Hz), 8.03 (1H, d, J 7.4 Hz), 8.27 (1H, dd, J 2.1, 9.1 Hz), 8.41 (1H, d, J 5.3 Hz), 8.57 (1H, d, J 1.8 Hz), 8.95 (1H, d, J 2.1 Hz) and 9.45 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06093716
Source datasetuspto-grants-2000_07
ORD IDord-a2f3aafaf3d64bd1939be556e6186341
Source noteuspto-grants-2000_07