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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2181467Generated: November 2, 2026

1,1'-Carbonyldiimidazole → HCID 10216123, compound

https://huagongshe.com/reaction/2181467

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantEthanol, 2-(aminooxy)-HCID 3014186—
ReactantHCID 22025611HCID 22025611—
ProductHCID 10216123HCID 1021612369%

Reaction Steps

The title compound was prepared from reaction of the product of Example 25, Step C, 3,4-difluoro-2-[[2-fluoro-4-(3-methoxypropyl)phenyl]amino]benzoic acid with CDI and 2-(aminooxy)ethanol, by the general procedure of Example 1, Step E, then purified by flash column chromatography on silica gel (50% EtOAc/hexanes) to give 3,4-difluoro-2-[[2-fluoro-4-(3-methoxypropyl)phenyl]-amino]-N-(2-hydroxyethoxy)benzamide as a cream solid (69%); m.p. (Et2O/hexanes) 136-137° C. 1H NMR [400 MHz, (CD3)2SO] δ 11.85 (br s, 1 H), 8.77 (br s, 1 H), 7.43-7.36 (m, 1 H), 7.15-7.00 (m, 2 H), 6.95-6.77 (m, 2 H), 4.71 (br s, 1 H), 3.85 (t, J=4.8, 2 H), 3.56 (t, J=4.8, 2 H), 3.33 (t, J=6.4 Hz, 2 H), 3.23 (s, 3 H), 2.56 (t, J=7.7 Hz, 2 H), 1.80-1.71 (m, 2 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06891066B2
Source datasetuspto-grants-2005_05
ORD IDord-129a91ddfcf14d9e985c7481d2f03a03
Source noteuspto-grants-2005_05