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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827476Generated: October 31, 2026

Triethylamine → HCID 10431638, compound

https://huagongshe.com/reaction/1827476

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-MethylallylamineHCID 76141—
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-Pyridin-2-yl-vinyl)-1H-indazol-6-ylamino]-benzoic acidHCID 69352963—
SolventDimethylformamideHCID 6228—
ProductHCID 10431638HCID 10431638130.8%

Reaction Steps

A solution of 2-[3-(2-Pyridin-2-yl-vinyl)-1H-indazol-6-ylamino]-benzoic acid (50.0 mg, 0.084 mmol), 2-methyl-allylamine (16.4 μL, 0.17 mmol), triethylamine (58 μl, 0.42 mmol), dissolved in DMF (0.8 mL), was treated with HATU (48 mg, 0.13 mmol). The mixture was stirred overnight, then purified by reverse phase HPLC yielding 45 mg (91%) of the title compound as a TFA salt (1.6 H2O, 1.3 TFA, effective MW=586.53). 1H NMR (DMSO-d6): δ 9.78 (1H, s), 8.72 (2H, m), 8.13 (4H, m), 7.70 (1H, d, J=7.1), 7.58 (2H, m), 7.41 (2H, m), 7.27 (1H, s), 7.06 (1H, d, J=7.1), 6.91 (1H, t, J=7.5), 4.42 (1H, m), 2.22 (2H, m), 2.08 (2H, m), 1.68 (2H, m). ESIMS (M+H+): 410.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07053107B2
Source datasetuspto-grants-2006_05
ORD IDord-b8f39352be2f43bd8f0bb8c641e5e32a
Source noteuspto-grants-2006_05