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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946845Generated: November 1, 2026

Ethyl Acetate → HCID 66771576, compound

https://huagongshe.com/reaction/1946845

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
ReactantHCID 59548935HCID 59548935—
SolventDichloromethaneHCID 6344—
ProductHCID 66771576HCID 6677157642%

Reaction Steps

A solution of sulfonyl chloride 32 (0.160 g, 0.50 mmol), tert-butyl piperazine-1-carboxylate (0.121 g, 0.65 mmol), and TEA (0.066 g, 0.65 mmol) in DCM (5 mL) was stirred overnight at room temperature. The reaction was monitored with TLC (25% EtOAc in hexanes). The reaction mixture was concentrated in vacuo and the residual was redissolved with a minimal amount of DCM and chromatographed on normal-phase silica to produce compound 33 as a white powder (0.099 g, 42.0% yield, 100.0% pure). 1H NMR (500 MHz, DMSO-d6): δ 8.24 (d, J=2 Hz, 1H), 8.00 (dd, J1=2 Hz, J2=8 Hz, 1H), 7.29 (d, J=8 Hz, 1H), 7.09 (d, J=8 Hz, 1H), 6.98 (s, 1H), 6.78 (d, J=8 Hz, 1H), 3.39 (m, 4H), 3.22 (m, 4H), 2.29 (s, 3H), 2.07 (s, 3H), 1.37 (s, 9H); MS (ESI, EI+): m/z=372 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399456B2
Source datasetuspto-grants-2013_03
ORD IDord-705c3c2681a642e7a88ba9c8e0ac94de
Source noteuspto-grants-2013_03