Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1474443Generated: October 30, 2026

Acetic Acid → HCID 178467936, compound

https://huagongshe.com/reaction/1474443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPiperidineHCID 8082—
Reactantsodium (1Z)-1-cyanoprop-1-en-2-olateHCID 23687916—
ReactantHCID 178434286HCID 178434286—
SolventDichloromethaneHCID 6344—
ProductHCID 178467936HCID 17846793650%

Reaction Steps

A mixture of 5.0 g (31.2 mmol) 3-methyl-1H-indazole-5-carbaldehyde (Example 1A), 3.61 g (34.3 mmol) sodium (1Z)-1-cyanoprop-1-en-2-olate, 2.23 ml (39 mmol) acetic acid and 0.31 ml (3.12 mmol) piperidine in dry dichloromethane (250 ml) containing 4 Å molecular sieve was stirred under reflux for 12 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 (3.5 g, 50% of th.) as a pale yellow solid which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018234B2
Source datasetuspto-grants-2015_04
ORD IDord-cbb355d7147240a09f43aabbfc52a551
Source noteuspto-grants-2015_04