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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827465Generated: October 27, 2026

Trifluoroacetic acid → 2-(3-[2-(5-Ethyl-pyridin-2-yl)-vinyl]-1H-indazol-6-ylamino)-N-prop-2-ynyl-benzamide

https://huagongshe.com/reaction/1827465

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantPropargylamineHCID 239041—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant2-{3-[2-(5-Ethyl-pyridin-2-yl)-vinyl]-1H-indazol-6-ylamino}-benzoic acidHCID 69354605—
SolventTolueneHCID 1140—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product2-(3-[2-(5-Ethyl-pyridin-2-yl)-vinyl]-1H-indazol-6-ylamino)-N-prop-2-ynyl-benzamideHCID 8659446166%

Reaction Steps

To 2-{3-[2-(5-Ethyl-pyridin-2-yl)-vinyl]-1H-indazol-6-ylamino}-benzoic acid (49 mg, 0.105 mmol) was added 2 mL of a 90:10:1 mixture of CH2Cl2:TFA:TES. The reaction was stirred at reflux for 1 hour, and then diluted with toluene (20 mL). The solvent was removed by rotary evaporation to yield a thick oil. The oil was dissolved in DMF (1 mL) and to this solution was added TEA (0.072 mL, 0.52 mmol), propargyl amine (0.014 mL, 0.208 mmol), and HATU (59 mg, 0.156 mmol). The reaction was stirred for 3 hours, and then purified by preparatory HPLC to yield the desired product (29 mg, 66%). 1H NMR (CDCL3-d): δ 9.83 (1H, s), 8.63 (2H, s), 8.04 (2H, m), 7.68 (2H, s), 7.47 (1H, m), 7.32 (1H, d, J=1.51 Hz), 7.10 (1H, dd, J1=8.67 Hz, J2=1.88 Hz), 6.93 (1H, m), 6.07 (2H, dd, J1=5.09 Hz, J2=2.26 Hz), 3.15 (1H, t, J=2.35 Hz), 2.97 (2H, s), 2.74 (1H, s), 2.29 (1H, s), 1.27 (3H, t, J=7.44 Hz)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07053107B2
Source datasetuspto-grants-2006_05
ORD IDord-629052a5ffb144d8a4eb4ccf082627c3
Source noteuspto-grants-2006_05