Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2305965Generated: November 1, 2026

HCID 18433429, compound → HCID 22728127, compound

https://huagongshe.com/reaction/2305965

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 18433429HCID 18433429—
SolventMethanolHCID 887—
ProductHCID 22728127HCID 22728127—

Reaction Steps

5-(4-Amino-2,6-dimethyl-phenoxy)-N-cyclobutyl-2-hydroxy-N-methyl-benzamide was prepared from N-cyclobutyl-5-(2,6-dimethyl-4-nitro-phenoxy)-2-hydroxy-N-methyl-benzamide according to a procedure analogous to that described in EXAMPLE 4, Step A. Methanol was used instead of ethanol as a co-solvent. The reaction mixture was hydrogenated for 2 hours. Then, the mixture was filtered through Celite® and concentrated, and the title product of Step F was used in the next step without purification. MS (APCI+) Calc.: 340.4, Found: 341.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06441015B2
Source datasetuspto-grants-2002_08
ORD IDord-d9167513394c4845b2b4b21a3425aed0
Source noteuspto-grants-2002_08