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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1625085Generated: November 1, 2026

1H-indazol-3-amine → HCID 65855926, compound

https://huagongshe.com/reaction/1625085

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-indazol-3-amineHCID 13399—
ReactantPotassium HydroxideHCID 14797—
ReactantSodium hydrideHCID 24758—
Reactant4-(Chloromethyl)-2-methyl-1,3-thiazole--hydrogen chloride (1/1)HCID 2734203—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductHCID 65855926HCID 6585592677%

Reaction Steps

A solution of 1H-indazol-3-amine (ABCR, 700 mg, 5.26 mmol) in anhydrous DMSO (10 ml) was added to a suspension of potassium hydroxide (PANREAC, 737 mg, 13.14 mmol) in anhydrous DMSO (40 mL) and this mixture was stirred for 10 min. A solution of 4-(chloromethyl)-2-methyl-1,3-thiazole hydrochloride (BUTTPARK, 776 mg, 5.26 mmol) and sodium hydride (ALDRICH, 126 mg, 5.26 mmol) in anhydrous DMSO (10 mL) was added dropwise to the mixture. Reaction was stirred at room temperature for 32 hours. Mixture of reaction was poured into water (100 mL) and extracted using DCM (4×100 mL). The combined organics were washed with water:brine (1:1) (100 mL) and dried over MgSO4 (anh), filtered and concentrated to dryness. Residue was purified using silica chromatography column using a linear gradient of DCM/MeOH (0% - - - >5%) as eluents to give the title compound 1-[(2-methyl-1,3-thiazol-4-yl)methyl]-1H-indazol-3-amine (988 mg, 4.04 mmol, 77% yield). 1H NMR (400 MHz, DMSO-d6) δ ppm: 7.67-7.69 (m, 1H), 7.40-7.43 (m, 1H), 7.23-7.28 (m, 1H), 7.07 (s, 1H), 6.90-6.90 (m, 1H), 5.46 (br s, 2H), 5.31 (s, 2H), 2.57 (s, 3H). [ES+MS] m/z 245 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08779153B2
Source datasetuspto-grants-2014_07
ORD IDord-e5c1b53163fd4661b0112c0af0d9d696
Source noteuspto-grants-2014_07