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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2069132Generated: November 2, 2026

2-methoxy-N-(4-(2-methoxy-4-nitrophenoxy)pyridin-2-yl)acetamide → N-(4-(4-Amino-2-methoxyphenoxy)pyridin-2-yl)-2-methoxyacetamide

https://huagongshe.com/reaction/2069132

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-methoxy-N-(4-(2-methoxy-4-nitrophenoxy)pyridin-2-yl)acetamideHCID 70921732—
ReactantHCID 178418361HCID 178418361—
CatalystPlatinumHCID 23939—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductN-(4-(4-Amino-2-methoxyphenoxy)pyridin-2-yl)-2-methoxyacetamideHCID 86660486—

Reaction Steps

A solution of 2-methoxy-N-(4-(2-methoxy-4-nitrophenoxy)pyridin-2-yl)acetamide (232 mg, 696 μmol) in a mixture of MeOH (30 mL) and AcOH (2.0 mL) was subjected to hydrogenation by passage through a Thales H-cube (1.0 mL min−1, 50° C., 55 mm 10% Pt/C Cat-Cart, full hydrogen mode) and was then evaporated in vacuo to afford the title compound, Intermediate H4 as an impure oily liquid; Rt 1.08 min (Method 2); m/z 304 (M+H)+ (ES+). This material, containing residual acetic acid was used directly, without further purification, in the next step (below).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299074B2
Source datasetuspto-grants-2012_10
ORD IDord-74fc1a0449c247968d779157ae2b2466
Source noteuspto-grants-2012_10