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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827468Generated: November 1, 2026

Triethylamine → HCID 11742351, compound

https://huagongshe.com/reaction/1827468

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantO-Allylhydroxylamine hydrochlorideHCID 3084724—
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 11742351HCID 1174235174%

Reaction Steps

A solution of 2-[3-(2-Pyridin-2-yl-vinyl)-1H-indazol-6-ylamino]-benzoic acid (50.0 mg, 0.084 mmol), O-allyl-hydroxylamine hydrochloride (18.3 mg, 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 25.5 mg (74%) of the title compound as a yellow solid. 1H NMR (DMSO-d6): δ 9.28 (1H, s), 8.67 (2H, d, J=3.4), 8.05 (4H, m), 7.48 (5H, m), 7.23 (1H, s), 7.04 (1H, d, J=7.6 Hz), 6.91 (1H, m), 3.69 (3H, s). ESIMS (M+H+): 386.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07053107B2
Source datasetuspto-grants-2006_05
ORD IDord-60722b4ce6f34817bf0c72004e78931a
Source noteuspto-grants-2006_05