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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2-[1-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-5-(3-nitro-pyrazol-1-ylmethyl)-oxazole | HCID 66928553 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-{2-[1-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-oxazol-5-ylmethyl}-1H-pyrazol-3-ylamine | HCID 66929442 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08288419B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-b1486c4bae5747519456e58fa13710c9 |
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| Source note | uspto-grants-2012_10 |
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