Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1256351Generated: October 31, 2026

N-Acetylhomopiperazine → HCID 44250829, compound

https://huagongshe.com/reaction/1256351

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-AcetylhomopiperazineHCID 4186202—
ReactantHCID 86652276HCID 86652276—
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-c]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 numberUS08461163B2
Source datasetuspto-grants-2013_06
ORD IDord-7f6c820309b84a409560523ea97228d5
Source noteuspto-grants-2013_06