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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2067276Generated: November 1, 2026

m-Aminoacetanilide → HCID 11554573, compound

https://huagongshe.com/reaction/2067276

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-AminoacetanilideHCID 7604—
ReactantHCID 11510648HCID 11510648—
ReactantHCID 68418335HCID 68418335—
ProductHCID 11554573HCID 11554573—

Reaction Steps

The reaction was carried out similarly as described in the preparation of compound 148, using compound 452 (0.13 mmol) and N-(3-amino-phenyl)-acetamide (0.13 mmol). The crude product was purified by continuous gradient flash chromatography using NH3(aq.)/MeOH/DCM 0:0:100, 1:9:90 as the eluent to afford the title compound as yellow solid. 13C NMR (DMSO-d6) δ 196.1, 168.2, 147.9, 145.6, 142.4, 142.0, 141.2, 140.1, 135.1, 135.0, 134.3, 131.9, 129.3, 126.0, 120.6, 120.2, 118.2, 117.6, 114.2, 112.7, 111.1, 110.0, 60.1, 29.1, 24.0, 22.1, 18.7

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08293772B2
Source datasetuspto-grants-2012_10
ORD IDord-2006465bc1874a7ca46cb5f5fc17c432
Source noteuspto-grants-2012_10