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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1273045Generated: October 27, 2026

Ethanolamine → [3-(4-Fluorophenyl)(1h-indazol-5-yl)]-n-(2-hydroxyethyl)carboxamide

https://huagongshe.com/reaction/1273045

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolamineHCID 700—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Reactant3-(4-Fluorophenyl)-1H-Indazole-5-Carboxylic AcidHCID 22260722—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product[3-(4-Fluorophenyl)(1h-indazol-5-yl)]-n-(2-hydroxyethyl)carboxamideHCID 2078905069%

Reaction Steps

The title compound was prepared as described in Example 76. To a solution of 3-(4-fluorophenyl)-1H-indazole-5-carboxylic acid (0.200 g, 0.781 mmol) in tetrahydrofuran (5 mL) was added 1-hydroxybenzotriazole hydrate (0.316 g, 2.34 mmol) followed by 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (0.449 g, 2.34 mmol), ethanolamine (0.141 mL, 2.34 mmol) and N,N-dimethylformamide (2 mL). The solution was stirred for 16 h at room temperature. Water (40 mL) was added and the solid was filtered and dried in a vacuum oven which gave the title compound (0.161 g, 69% yield): 1H NMR (DMSO-d6) δ 13.45 (s, 1H), 8.61 (t, 1H), 8.56 (s, 1H), 8.08 (AB quartet, 2H), 7.93 (dd, 1H), 7.62 (d, 1H), 7.40 (t, 2H), 4.76 (t, 1H), 3.54 (q, 2H), 3.80 (q, 2H); ES-MS (m/z) 300 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07208513B2
Source datasetuspto-grants-2007_04
ORD IDord-2abd689fc1b04623b9a3b1bd9868aec4
Source noteuspto-grants-2007_04