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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1047638Generated: November 1, 2026

1,2-Dimethoxyethane → Methyl 3-(2-hydroxypropan-2-yl)-1-(thiophen-3-yl)-1H-indazole-6-carboxylate

https://huagongshe.com/reaction/1047638

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantTetraethylammonium tetrahydroborateHCID 28251—
ReactantMethyl 3-(prop-1-en-2-yl)-1-(thiophen-3-yl)-1H-indazole-6-carboxylateHCID 66661623—
Catalystmeso-Tetraphenylporphine-Co(II)HCID 518893—
SolventMethanolHCID 887—
ProductMethyl 3-(2-hydroxypropan-2-yl)-1-(thiophen-3-yl)-1H-indazole-6-carboxylateHCID 6666152080%

Reaction Steps

Methyl 3-(prop-1-en-2-yl)-1-(thiophen-3-yl)-1H-indazole-6-carboxylate (1.0763 g, 3.61 mmol) was dissolved in dimethoxyethane (90 ml)/MeOH (90 ml) at 25° C. Cobalt(II) meso-tetraphenylporphine (25.6 mg, 0.038 mmol) and tetraethylammonium borohydride (1.316 g, 9.07 mmol) were added sequentially. The reaction mixture was allowed to stir for 1.25 h. The reaction was stopped, quenched by addition of saturated aqueous ammonium chloride (100 mL), and the mixture extracted with ethyl acetate (3×80 mL). The combined organic phases were washed with saturated aqueous sodium chloride (1×80 mL), dried (sodium sulfate), filtered, and the solvent evaporated under reduced pressure. The crude product was purified by flash chromatography (RediSep SiO2, 330 g column) on a CombiFlash Rf purification system eluting with ethyl acetate-hexanes (0-45%). The title compound (912.2 mg, 2.88 mmol, 80% yield) was recovered as an orange solid. LC-MS: [M+1]=317.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569512B2
Source datasetuspto-grants-2013_10
ORD IDord-18cb3265a838422c81948ecfad00141c
Source noteuspto-grants-2013_10