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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 713331Generated: October 29, 2026

Acetic Anhydride → Trifluoroacetic acid

https://huagongshe.com/reaction/713331

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 131734039HCID 131734039—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductTrifluoroacetic acidHCID 6422877%
ProductHCID 118159200HCID 118159200—

Reaction Steps

A solution of N-(tert-butyl)-3-(4-(2,4-difluorophenoxyl)piperidin-1-yl)-5,6,7,8-tetrahydropyrido[3,4-b]pyrazin-2-amine TFA salt (16 mg, 0.030 mmol), acetic anhydride (5.7 μL, 0.060 mmol), and DIPEA (15.8 μL, 0.090 mmol) in DCM (151 μL) was stirred at room temperature overnight. The crude reaction mixture was diluted in DMF, filtered through a hydrophilic PTFE 0.45 μm filter (Millipore® Millex-LCR), and purified via HPLC Method A to give the title compound as a TFA salt (15 mg) as a clear oil. 1H NMR (400 MHz, methanol-d4, mixture of rotamers) δ ppm 1.48 (s, 9H), 1.87-1.98 (m, 2H), 2.07-2.17 (m, 2H), 2.19 (s, 1.3H), 2.21 (s, 1.7H), 2.74 (t, J=5.9 Hz, 0.9H), 2.84 (t, J=5.9 Hz, 1.1H), 2.97 (ddd, J=12.4, 8.6, 3.3 Hz, 2H), 3.33-3.37 (m, 2H), 3.80 (t, J=5.9 Hz, 1.1H), 3.85 (t, J=5.9 Hz, 0.9H), 4.43-4.51 (m, 1H), 4.53 (d, J=1.3 Hz, 2H), 6.88 (ddddd, J=9.1, 8.1, 2.9, 1.9, 0.8 Hz, 1H), 6.95-7.02 (m, 1H), 7.18 (td, J=9.2, 5.3 Hz, 1H); ESI-MS m/z [M+H]+ 460.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181249B2
Source datasetuspto-grants-2015_11
ORD IDord-d8b2ed4840b64a00921d163a6ae21608
Source noteuspto-grants-2015_11