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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-(cyclopropylmethyl)hydroxylamine hydrochlorideHCID 11557279—
ReactantHCID 136009249HCID 136009249—
SolventEthanolHCID 702—
ProductHCID 136359927HCID 13635992780%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426411B2
Source datasetuspto-grants-2013_04
ORD IDord-e4d744a9eb0c450abfbf56ad211c882f
Source noteuspto-grants-2013_04