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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1466345Generated: November 2, 2026

HCID 67447598, compound → HCID 178520034, compound

https://huagongshe.com/reaction/1466345

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67447598HCID 67447598—
ReactantHCID 178527019HCID 178527019—
CatalystNickelHCID 935—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
ProductHCID 178520034HCID 17852003430%

Reaction Steps

To a solution of 6-((1R*,2S*)-2′-oxospiro[cyclopropane-1,3′-indoline]-2-yl)-1H-indazole-3-carbonitrile (1 g, 3.3 mmol) in pyridine (30 mL) acetic acid (8 mL) and water (8 mL) and Raney Nickel (1 g). Sodium hypophosphite (1.8 g, 21 mmol) was dissolved in water (10 mL) and added dropwise and the reaction was stirred overnight. The product was extracted into ethyl acetate (300 mL), washed with brine (50 mL), dried over MgSO4 and concentrated to dryness. The residue was purified by silica gel chromatography (95:5 CH2Cl2/MeOH) to give the title compound as a yellow solid (300 mg, 30%). 1H NMR (400 MHz, CD3OD) δ 10.17 (s, 1H), 8.10 (d, J=8.3 Hz, 1H), 7.55 (s, 1H), 7.17 (d, J=8.5 Hz, 1H) 7.08-7.04 (m, 1H), 6.94 (d, J=8.3 Hz, 1H), 6.56 (t, J=7.6 Hz, 1H), 5.93 (d, J=7.5 Hz, 1H), 3.38-3.34 (m, 1H), 2.27-2.17 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999968B2
Source datasetuspto-grants-2015_04
ORD IDord-b77a62c4a38a47a5a669a8ef82d0fb91
Source noteuspto-grants-2015_04