Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2055211Generated: October 31, 2026

N-benzyloxy-N-{4,4-dimethyl-1-[N'-(4-trifluoromethyl-pyrimidin2-yl)-hydrazinocarbonyl]-cyclohexylmethyl}-formamide → N-{4,4-Dimethyl-1-[N'-(4-trifluoromethyl-pyrimidin-2-yl)-hydrazinocarbonyl]-cyclohexylmethyl}-N-hydroxy-formamide

https://huagongshe.com/reaction/2055211

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-benzyloxy-N-{4,4-dimethyl-1-[N'-(4-trifluoromethyl-pyrimidin2-yl)-hydrazinocarbonyl]-cyclohexylmethyl}-formamideHCID 86606478—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductN-{4,4-Dimethyl-1-[N'-(4-trifluoromethyl-pyrimidin-2-yl)-hydrazinocarbonyl]-cyclohexylmethyl}-N-hydroxy-formamideHCID 1174959074%

Reaction Steps

To a solution of N-benzyloxy-N-{4,4-dimethyl-1-[N′-(4-trifluoromethyl-pyrimidin2-yl)-hydrazinocarbonyl]-cyclohexylmethyl}-formamide (0.11 g, 0.23 mmol) in methanol (10 mL) was added 10% Pd/C (0.032 g). The reaction mixture was subjected to hydrogenation for 1 h at room temperature. The reaction mixture was then filtered through a pad of Celite@, and washed with methanol (20 mL). Removal of the solvent provided the title compound as a white solid (0.066 g, 74%). MH+390.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07332485B2
Source datasetuspto-grants-2008_02
ORD IDord-8f2da3e3c4914c2b93f696f2a8940201
Source noteuspto-grants-2008_02