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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 860820Generated: October 31, 2026

Hydrochloric Acid → HCID 66647628, compound

https://huagongshe.com/reaction/860820

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTrifluoroacetic acidHCID 6422—
ReactantTrifluoroacetic acid methylene chlorideHCID 21863450—
ReactantHCID 67908624HCID 67908624—
ReactantHCID 70166724HCID 70166724—
ReactantSulfuric acid, mixt. with nitric acidHCID 71777668—
ReactantHCID 86601405HCID 86601405—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66647628HCID 66647628—

Reaction Steps

Fused pyrazoline (III) can be converted to its corresponding pyrazole-pyridinone (IV) by treatment with an acid. This deamination reaction is preferably performed in the presence of a strong acid (e.g., trifluoroacetic acid (TFA), sulfuric acid nitric acid, and hydrochloric acid (HCl)). An aprotic solvent may be used (e.g., CH2Cl2 or THF). As one of ordinary skill in the art recognizes, some acids are usually available in the presence of a second solvent. For example, 6N HCl can be available in isopropyl alcohol (IPA). 2N HCl can be available as an aqueous solution. Thus, the second solvent, if present, will depend on the acid used. Preferably, the second solvent is isopropyl alcohol or water. The reaction can be conducted from about 5° C. to reflux of the solvent. Preferably, when TFA, either neat or in CH2Cl2, is used, the reaction is conducted at a temperature of from 5° C. to room temperature (approximately 25° C.). Preferably, when HCl (e.g., 2N or 6N) is used, the reaction solvent is THF and the reaction is conducted at about the reflux temperature of THF. Preferred acids or acid solvent combinations are: TFA (neat), TFA/CH2Cl2, 6N HCl/isopropyl alcohol/THF, and 2N HCl/water/THF.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07153960B2
Source datasetuspto-grants-2006_12
ORD IDord-0a2f012a0c8243b1a57d4a91d455005c
Source noteuspto-grants-2006_12