HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1157768Generated: October 30, 2026
O-Methylhydroxylamine hydrochloride → HCID 49770162, compound
https://huagongshe.com/reaction/1157768
Participants
| Role | Name | HCID | Charge |
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| Reactant | O-Methylhydroxylamine hydrochloride | HCID 521874 | — |
| Reactant | HCID 49770160 | HCID 49770160 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 49770162 | HCID 49770162 | — |
Reaction Steps
To a suspension of 1-(7-acetyl-4-fluoro-1H-pyrrolo[2,3-c]pyridin-3-yl)-2-(4-(1-phenyl-1H-tetrazol-5-yl)piperazin-1-yl)ethane-1,2-dione (0.05 g, 0.11 mmol) in EtOH (10 mL) was added methoxylamine hydrochloride (0.05 g, 0.60 mmol). The mixture was heated to reflux for 1 h, and was then cooled to rt, and concentrated in vacuo. The residue was diluted with MeOH, and the solids that formed were collected and washed with water. The title compound was isolated as a light-yellow solid (0.025 g). LCMS: m/e 492.4 (M+H)+, ret time 2.068 min (method 2). 1H NMR (500 MHz, DMSO-D6) δ ppm 12.02 (s, 1H) 8.36 (d, J=2.14 Hz, 1H) 8.27 (d, J=3.36 Hz, 1H) 7.56-7.71 (m, 5H) 4.13-4.16 (m, 3H) 3.68-3.73 (m, 2H) 3.43-3.48 (m, 2H) 3.29-3.36 (m, 2H) 3.13-3.18 (m, 2H) 2.36 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07807676B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-8a1c866121e14dc389e32fb35b6c6b95 |
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| Source note | uspto-grants-2010_10 |
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