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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1484552Generated: October 30, 2026

Acetic Acid → HCID 178437998, compound

https://huagongshe.com/reaction/1484552

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPiperidineHCID 8082—
Reactantsodium (1Z)-1-cyanoprop-1-en-2-olateHCID 23687916—
ReactantHCID 178437999HCID 178437999—
SolventDichloromethaneHCID 6344—
ProductHCID 178437998HCID 17843799888%

Reaction Steps

A mixture of 0.50 g (2.87 mmol) 3-ethyl-1H-indazole-5-carbaldehyde (Example 10A), 0.33 g (3.16 mmol) sodium (1Z)-1-cyanoprop-1-en-2-olate, 0.21 ml (3.6 mmol) acetic acid and 0.028 ml (0.29 mmol) piperidine in dry dichloromethane (25 ml) containing 4 Å molecular sieve was stirred under reflux for 16 h. Upon cooling, a precipitate was formed which was collected by filtration and washed with saturated aqueous sodium bicarbonate solution and water. The solid was dissolved in ethanol, and the molecular sieve was filtered off. The filtrate was concentrated under reduced pressure, and the residue was treated with ethyl acetate and saturated aqueous sodium carbonate solution. The organic layer was washed with water, dried, and concentrated under reduced pressure to afford the title compound (0.60 g, 88% of th.) as a pale yellow solid which was used in subsequent steps without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422263B2
Source datasetuspto-grants-2016_08
ORD IDord-8150b60911f9436c9257db529fe88e9a
Source noteuspto-grants-2016_08