Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1161992Generated: October 28, 2026

HCID 21864857, compound → HCID 66894206, compound

https://huagongshe.com/reaction/1161992

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 21864857HCID 21864857—
ReactantHCID 66891841HCID 66891841—
ProductHCID 66894206HCID 66894206—

Reaction Steps

Reduction of the nitro group in N,N-diethyl-2-[4-(5-nitro-1-benzofuran-7-yl)piperazin-1-yl]acetamide (0.3 g, 0.83 mmol; Intermediate 22) was performed according to the procedure of Intermediate 10. Yield: 0.19 g (70%). This material was used in the next step without further purification. MS (ESI+) m/z 331.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820675B2
Source datasetuspto-grants-2010_10
ORD IDord-211ed25683a3458b9f750fa4f28a6ced
Source noteuspto-grants-2010_10