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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1474508Generated: November 1, 2026

Indazole-3-carboxylic acid → 1H-Indazole-3-carboxylic acid (4-benzyloxy-phenyl)-amide

https://huagongshe.com/reaction/1474508

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndazole-3-carboxylic acidHCID 78250—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Benzyloxyaniline hydrochlorideHCID 2723831—
ReactantMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
SolventDimethylformamideHCID 6228—
Product1H-Indazole-3-carboxylic acid (4-benzyloxy-phenyl)-amideHCID 9314292—

Reaction Steps

DIEA (9.3 mL, 53.4 mmol) was added to a solution of 4-benzyloxyaniline hydrochloride (4.0 g, 17.0 mmol), indazole-3-carboxylic acid (2.89 g, 17.8 mmol) and HBTU (7.1 g, 18.7 mmol) in DMF (60 mL), and the resulting solution was stirred at ambient temperature for 24 hours. The solution was heated to 70° C. for 4 hours, and then poured into a mixture of saturated aqueous sodium bicarbonate on ice. The product, an off white solid, 6.0 g, was collected by filtration, washed with water and used without further purification in the subsequent reaction. MS m/z 344 (MH+). 1H NMR(DMSO-d6) δ 5.11 (s, 2H), 7.02 (d, 2H), 7.26-7.48 (m, 7H), 7.67 (d, 1H), 7.75 (d, 2H), 7.81 (d, 1H), 8.24 (d, 1H) and 10.24 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018241B2
Source datasetuspto-grants-2015_04
ORD IDord-4344833953154e06b3e9640829768522
Source noteuspto-grants-2015_04