Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1353823Generated: November 3, 2026

Triethylamine → HCID 178483327, compound

https://huagongshe.com/reaction/1353823

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-(Dimethylamino)acetohydrazideHCID 68319—
Reactantethoxy[3-(4-fluorophenyl)(1H-indazol-5-yl)]methaneamine hydrochlorideHCID 21101187—
SolventEthanolHCID 702—
ProductHCID 178483327HCID 17848332792.1%

Reaction Conditions

Temperature75 °C

Reaction Steps

To a solution of ethoxy[3-(4-fluorophenyl)(1H-indazol-5-yl)]methaneamine hydrochloride (200 mg, 0.62 mmol), N-amino-2-(dimethylamino)acetamide (147.5 mg, 0.95 mmol), and molecular sieves in ethanol was added triethylamine (0.25 mL, 1.86 mmol). The reaction was allowed to stir under a nitrogen atmosphere at 75° C. overnight. The reaction was filtered using a fritted funnel and the filtrate was concentrated. This was purified by semi-preprative HPLC. The material was taken up in ethyl acetate and washed with aqueous sodium bicarbonate. This organic layer was dried with magnesium sulfate, filtered and concentrated to yield the title compound (192 mg, 23% yield). 1H NMR (CD3OD) δ 8.7 (s, 1H), 8.0–8.1 (m, 3H), 7.7 (d, 1H), 7.25 (t, 2H), 4.5 (s, 2H), 3.0 (s, 6H), ES-MS (m/z) 337 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07220771B2
Source datasetuspto-grants-2007_05
ORD IDord-de43b2037a134752a379de3d630bd644
Source noteuspto-grants-2007_05