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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2055210Generated: October 31, 2026

N-Benzyloxy-N-{1-[N'-(4-trifluoromethyl-pyrimidin-2-yl)-hydrazinocarbonyl]-cyclohexylmethyl}-formamide → N-Hydroxy-N-{1-[N'-(4-trifluoromethyl-pyrimidin-2-yl)-hydrazinocarbonyl]-cyclohexylmethyl}-formamide

https://huagongshe.com/reaction/2055210

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Benzyloxy-N-{1-[N'-(4-trifluoromethyl-pyrimidin-2-yl)-hydrazinocarbonyl]-cyclohexylmethyl}-formamideHCID 86606473—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductN-Hydroxy-N-{1-[N'-(4-trifluoromethyl-pyrimidin-2-yl)-hydrazinocarbonyl]-cyclohexylmethyl}-formamideHCID 1121062785%

Reaction Steps

To a solution of N-benzyloxy-N-{1-[N′-(4-trifluoromethyl-pyrimidin-2-yl)-hydrazinocarbonyl]-cyclohexylmethyl}-formamide (0.066 g, 0.15 mmol) in ethanol (5 mL) was added 10% Pd/C (0.03 g). The reaction mixture was subjected to hydrogenation for 3 h at room temperature. The reaction mixture was then filtered through a pad of Celite@, and washed with ethanol (20 mL). Removal of the solvent provided the title compound as a white solid (0.045 g, 85%). MH+362.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07332485B2
Source datasetuspto-grants-2008_02
ORD IDord-a31f773860984d1d8d97d92448222e7c
Source noteuspto-grants-2008_02