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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1714432Generated: October 29, 2026

3-Aminobenzyl alcohol → HCID 86591964, compound

https://huagongshe.com/reaction/1714432

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Aminobenzyl alcoholHCID 80293—
ReactantHCID 18445515HCID 18445515—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86591964HCID 86591964—

Reaction Steps

2-(Imidazole-1-carbothioyl)-5,6-dimethoxy-indan-1-one, Intermediate B, (1.0 g, 3.3 mmol) was mixed with 3-aminobenzyl alcohol (0.40 g, 3.3 mmol), and 30 mL THF in a flask. 5,6-Dimethoxy-1-oxo-indan-2-carbothioic acid (3-hydroxymethyl-phenyl)-amide was obtained after stirring the reaction mixture for 4 hours at room temperature. HPLC/MS m/z 358 (M+H)+. The intermediate was not isolated, the mixture was mixed with hydrazine (0.13 mL, 4 mmol), and acetic acid (2-3 drops). The reaction was heated at 78° C. for 12 hours. The reaction solution was then diluted with ethyl acetate, washed with water, and dried over Na2SO4. The solvent was removed and the title compound was purified by HPLC with a C-18 reversed phase column and CH3CN—H2O-TFA as gradient solvents. The title compound, [3-(6,7-Dimethoxy-2,4-dihydro-indeno[1,2-c]pyrazol-3-ylamino)-phenyl]-methanol, Compound 36, was obtained as a solid TFA salt. MS m/z 338 (M+H)+; HPLC:100% (uv 214 mu); 1HNMR (DMSO-d6): 3.40(s, 2H), 4.54(s, 2H), 6.81 (d, 1H), 7.02 (d, 1H), 7.14(s, 1H), 7.22(d, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795440B2
Source datasetuspto-grants-2010_09
ORD IDord-ba8495e8e31a43b385a3eb4d45f78ca7
Source noteuspto-grants-2010_09