HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 215878Generated: October 31, 2026
Hydrazine hydrate (1:1) → N-{(1S,2R,3S,4R)-4-[2-(4-Amino-pyrazol-1-yl)-6-(2,2-diphenyl-ethylamino)-purin-9-yl]-2,3-dihydroxy-cyclopentyl}-2-hydroxy-acetamide
https://huagongshe.com/reaction/215878
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | N-{(1S,2R,3S,4R)-4-[6-(2,2-diphenyl-ethylamino)-2-(4-nitro-pyrazol-1-yl)-purin-9-yl]-2,3-dihydroxy-cyclopentyl}-2-hydroxy-acetamide | HCID 66630082 | — |
| Catalyst | Iron chloride (FeCl3) | HCID 24380 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-{(1S,2R,3S,4R)-4-[2-(4-Amino-pyrazol-1-yl)-6-(2,2-diphenyl-ethylamino)-purin-9-yl]-2,3-dihydroxy-cyclopentyl}-2-hydroxy-acetamide | HCID 66630381 | — |
Reaction Steps
The title compound can be prepared by dissolving N-{(1S,2R,3S,4R)-4-[6-(2,2-diphenylethylamino)-2-(4-nitro-pyrazol-1-yl)-purin-9-yl]-2,3-dihydroxy-cyclopentyl}-2-hydroxy-acetamide (Intermediate QD) in methanol and adding a 2:1 by mass mixture of activated carbon and iron (III) chloride (40 mol % with respect to the substrate), followed by a large excess (100-fold with respect to the substrate) of hydrazine monohydrate. The resulting mixture is stirred at 65° C. for 3 hours, then filtered, before being concentrated under reduced pressure. Trituration of the residue with petroleum ether and subsequent filtration would give the desired product as a colourless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08193164B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-9e75773647df4c68bbeaa49a9e85166b |
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| Source note | uspto-grants-2012_06 |
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