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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2400303Generated: November 3, 2026

Trifluoroacetic acid → HCID 69092880, compound

https://huagongshe.com/reaction/2400303

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 58608394HCID 58608394—
ReactantHCID 70144271HCID 70144271—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 69092880HCID 6909288055.7%

Reaction Conditions

Temperature50 °C

Reaction Steps

As shown in Scheme 2, a mixture of intermediate 1 of Scheme 2 (16 mg) and N1-isopropyl-3-methoxybenzene-1,4-diamine (15 mg, prepared from WO 2006/021548) in dioxane (1.0 mL) with catalytic trifluoroacetic acid was stirred overnight at 50° C. The crude was concentrated under reduced pressure and purified using HPLC (TFA modifier) to give the title compound (8 mg) as a TFA salt. 1H-NMR (DMSO-d6, 400 MHz) δ 10.12 (s, 1H), 8.49 (br, 1H), 8.24 (s, 1H), 8.06 (s, 1H), 7.71 (br, 1H), 7.47 (d, J=6.4 Hz, 1H), 7.23 (m, 3H), 6.44 (dd, J=10.0, 16.8 Hz, 1H), 6.23 (m, 2H), 5.91 (m, 1H), 5.75 (dd, J=1.6, 10.0 Hz, 1H), 5.21 (m, 1H), 3.68 (s, 3H), 1.10 (d, J=6.0 Hz, 1H); calculated mass for C24H25F3N6O2: 486.2. found: 486.9 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796255B2
Source datasetuspto-grants-2014_08
ORD IDord-1c4497f8744f4f6e8df4a83d2313205d
Source noteuspto-grants-2014_08