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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 574641Generated: October 29, 2026

Tributylphosphine → HCID 71515892, compound

https://huagongshe.com/reaction/574641

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylphosphineHCID 13831—
Reactant1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
Reactant(S)-(+)-1-IndanolHCID 6971242—
ReactantHCID 57076369HCID 57076369—
SolventTolueneHCID 1140—
ProductHCID 71515892HCID 71515892—

Reaction Conditions

Temperature80 °C

Reaction Steps

According to Scheme 7: A mixture of 1-[3-(4-fluoro-phenyl)-1,4,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-5-yl]-ethanone (3b) (0.2 g, 0.771 mmol), tri-n-butylphosphine (0.312 g, 1.54 mmol), 1,1′-(azodicarbonyl)dipiperidine (0.389 g, 1.54 mmol) and (S)-1-indanol in dry toluene (2.5 ml) was stirred at 80° C. for 2 h. Solvents were evaporated in vacuo. The crude product was purified by reverse phase HPLC (CH3CN/water gradient with 0.1% trifluoroacetic acid) to give 81 mg of 1-[(R)-3-(4-fluoro-phenyl)-1-indan-1-yl-1,4,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-5-yl]-ethanone (12a)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09034897B2
Source datasetuspto-grants-2015_05
ORD IDord-bf78d23c252b4bec8f81c3ddac118741
Source noteuspto-grants-2015_05