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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 736671Generated: October 29, 2026

Trifluoroacetic acid → HCID 57850178, compound

https://huagongshe.com/reaction/736671

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 57850041HCID 57850041—
SolventDichloromethaneHCID 6344—
ProductHCID 57850178HCID 57850178130.2%

Reaction Steps

To a solution of [(S)-2-(4-{2-[6-Amino-8-(6-bromo-benzo[1,3]dioxol-5-ylsulfanyl)-purin-9-yl]-ethyl}-piperidin-1-yl)-1-methyl-2-oxo-ethyl]-carbamic acid tert-butyl ester (0.014 g, 0.021 mmol) in DCM (3 mL) was added drop wise TFA (100 μL) and the resulting mixture was stirred for overnight at room temperature. After concentration under reduced pressure, the residual TFA was removed to afford a title product (0.015 g) as a TFA salt. 1H NMR (CD3OD) δ 8.34 (s, 1H), 7.28 (s, 1H), 7.23 (s, 1H), 6.09 (s, 2H), 4.54-4.44 (m, 2H), 4.39 (t, J=7.42 Hz, 2H), 3.85 (broad d, J=13.2 Hz, 1H), 3.19-3.08 (m, 1H), 2.75-2.63 (m, 1H), 2.00-1.80 (m, 4H), 1.70-1.58 (m, 1H), 1.44 (dd, J=14.8, 7.0 Hz, 3H), 1.35-1.13 (m, 2H); LC-MS [M+H]+ 548.2

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07595401B2
Source datasetuspto-grants-2009_09
ORD IDord-7262b351f5f040d49169296bfc4cb248
Source noteuspto-grants-2009_09