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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2055212Generated: November 2, 2026

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

https://huagongshe.com/reaction/2055212

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Benzyloxy-N-{1-[N'-(4-trifluoromethyl-pyrimidin-2-yl)-hydrazinocarbonyl]-cycloheptylmethyl}-formamideHCID 86606480—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductN-Hydroxy-N-{1-[N'-(4-trifluoromethyl-pyrimidin-2-yl)-hydrazinocarbonyl]-cycloheptylmethyl}-formamideHCID 1147430575%

Reaction Steps

To a solution of N-benzyloxy-N-{1-[N′-(4-trifluoromethyl-pyrimidin-2-yl)-hydrazinocarbonyl]-cycloheptylmethyl}-formamide (0.11 g, 0.24 mmol) in methanol (10 mL) was added 10% Pd/C (0.03 g). The reaction mixture was subjected to hydrogenation for, 0.25 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 (0.067 g, 75%). MH+376.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07332485B2
Source datasetuspto-grants-2008_02
ORD IDord-1a0c8ec6a48846c8872fe834cd6100f8
Source noteuspto-grants-2008_02