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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1409192Generated: October 30, 2026

N-Acetylhomopiperazine → HCID 44250829, compound

https://huagongshe.com/reaction/1409192

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-AcetylhomopiperazineHCID 4186202—
ReactantHCID 86652274HCID 86652274—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 44250829HCID 4425082951.3%

Reaction Steps

In a 2 mL microwave vial was placed N-(7-chloro-2-cyclopropylpyrazolo[1,5-a]pyrimidin-5-yl)-4-(2-hydroxypropan-2-yl)benzamide (2H, 75 mg, 0.21 mmol) and N-acetylhomopiperazine (59 mg, 0.42 mmol). To the sealed vial was then added NMP (2 ml) and the mixture was then heated in the microwave at 120° C. for 30 minutes. After cooling to room temperature, the reaction mixture was partitioned between brine and EtOAc. The aqueous layer was extracted once more with EtOAc, and the combined organic layers were dried over MgSO4, filtered and concentrated in vacuo. The crude product was purified by recrystallization from ether and EtOAc to give the titled compound (50 mg, 51% yield) as an off-white solid. ESI-MS: m/z 465 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921358B2
Source datasetuspto-grants-2014_12
ORD IDord-7fcf27f16e5648928170d30f212000b7
Source noteuspto-grants-2014_12