Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504597Generated: October 30, 2026

1-Isopropylpiperazine → HCID 86730056, compound

https://huagongshe.com/reaction/1504597

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-IsopropylpiperazineHCID 78013—
ReactantHCID 86730055HCID 86730055—
SolventDichloromethaneHCID 6344—
ProductHCID 86730056HCID 8673005610.1%

Reaction Steps

To a solution of 1-(5-carbamoylpyridin-2-yl)-azetidin-3-yl 4-nitrophenyl carbonate (0.36 g, 1 mmol) in DCM (5 mL) under nitrogen was added 1-isopropylpiperazine (0.13 g, 1 mmol). The resulting solution was stirred under N2 at room temperature for 24 h. The reaction mixture was then filtered and the filter cake was washed with DCM. The combined filtrates were concentrated to afford the crude product. After further purified by preparative HPLC, the title compound (35 mg, 10%) was obtained as a yellow solid. [1HNMR (500 MHz, CDCl3) δ8.58 (d, 1H), 7.96 (dd, 1H), 7.76 (s, 1H), 7.77 (s, 1H), 7.15 (s, 1H), 6.41 (d, 1H), 5.21 (m, 1H), 4.32 (m, 2H), 3.92 (m, 2H), 3.41 (m, 4H), 2.65 (m, 1H), 2.40 (m, 4H), 0.95 (d, 6H); LCMS RtA=1.59 min, [M+H]+=348.2].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216182B2
Source datasetuspto-grants-2015_12
ORD IDord-c80b866830254c9d81ac25982a7f7ae2
Source noteuspto-grants-2015_12