HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1969657Generated: October 30, 2026
O-(cyclopropylmethyl)hydroxylamine hydrochloride → HCID 136359927, compound
https://huagongshe.com/reaction/1969657
Participants
| Role | Name | HCID | Charge |
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| Reactant | O-(cyclopropylmethyl)hydroxylamine hydrochloride | HCID 11557279 | — |
| Reactant | HCID 136009249 | HCID 136009249 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 136359927 | HCID 136359927 | 80% |
Reaction Steps
To a solution of (3R,4S)-3-ethyl-4-(6H-pyrrolo[2,3-e][1,2,4]triazolo[4,3-a]pyrazin-1-yl)cyclopentanone (0.05 g, 0.19 mmol, Example #AA.1.59) in EtOH (1 mL) was added TEA (0.04 mL, 0.28 mmol) and O-(cyclopropylmethyl)hydroxylamine hydrochloride (0.02 g, 0.19 mmol, Huhu Technologies). The reaction mixture was stirred for about 18 h at ambient temperature. Additional O-(cyclopropylmethyl)hydroxylamine hydrochloride (0.02 g, 0.19 mmol, Huhu Technologies) was added. The reaction was stirred at ambient temperature for about 5 h. The solvent was removed under reduced pressure. The crude material was purified by silica gel chromatography eluting with a gradient of 1-10% MeOH in DCM to afford (3R,4S)-3-ethyl-4-(6H-pyrrolo[2,3-e][1,2,4]triazolo[4,3-a]pyrazin-1-yl)cyclopentanone O-cyclopropylmethyl oxime (0.051 g, 80%): LC/MS (Table 1, Method a) Rt=1.94 min; MS m/z: 339 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08426411B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-e4d744a9eb0c450abfbf56ad211c882f |
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| Source note | uspto-grants-2013_04 |
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