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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2065060Generated: October 26, 2026

Nitrogen → 1-{2-[1-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-oxazol-5-ylmethyl}-1H-pyrazol-3-ylamine

https://huagongshe.com/reaction/2065060

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-[1-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-5-(3-nitro-pyrazol-1-ylmethyl)-oxazoleHCID 66928553—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product1-{2-[1-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-oxazol-5-ylmethyl}-1H-pyrazol-3-ylamineHCID 66929442—

Reaction Conditions

Temperature85 °C

Reaction Steps

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of 2-[1-(tert-butyl-dimethyl-silanyloxy)-ethyl]-5-(3-nitro-pyrazol-1-ylmethyl)-oxazole (219 mg, 0.62 mmol), iron powder (105 mg, 1.86 mmol) and NH4Cl (168 mg, 3.11 mmol) in a mixture of EtOH (2.0 mL) and water (1.0 mL) was stirred at 85° C. for 15 min. The reaction mixture was filtered while hot and concentrated under reduced pressure. CH2Cl2 (10 mL) was added followed by water (10 mL). The aq. layer was extracted with CH2Cl2 (2×10 mL) and the combined org. extracts were dried over MgSO4, filtered, and the solvents were removed under reduced pressure to give the title compound as a yellow oil. LC-MS-conditions 02: tR=0.89 min; [M+H]+=323.42.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288419B2
Source datasetuspto-grants-2012_10
ORD IDord-b1486c4bae5747519456e58fa13710c9
Source noteuspto-grants-2012_10