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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2096512Generated: October 30, 2026

N-methylhydroxylamine hydrochloride → HCID 58424550, compound

https://huagongshe.com/reaction/2096512

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-methylhydroxylamine hydrochlorideHCID 77906—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 178511917HCID 178511917—
SolventMethanolHCID 887—
ProductHCID 58424550HCID 584245503.1%

Reaction Steps

To a solution of methylhydroxylamine HCl salt (17 mg, 0.2 mmol) in anhydrous MeOH (2 mL) was added NaOMe (25% in MeOH (Wt. %), 0.10 mL, 0.2 mmol), followed by (E)-N-(6-(3-cyanophenyl)-2-(pyridine-3-yl)chroman-4-ylidene)cyanamide (70 mg, 0.2 mmol). After stirring for 10 mins, the solvent was removed in vacuo. The resulting residue was redissolved in DCM (5 mL). The mixture was filtered, and the solvent was removed to give the residue, which was purified by preparative TLC and preparartive HPLC to give 3-(3′-amino-2′-methyl-2-(pyridine-3-yl)-2′H-spiro[chroman-4,5′-[1,2,4]oxadiazole]-6-yl)benzonitrile (2.5 mg, 3%). 1H-NMR (MeOD): 2.40-2.47 (t, 1H), 2.92-3.16 (m, 1H), 3.46 (s, 3H), 5.61-5.69 (m, 1H), 7.21 (m, 1H), 7.64-7.67 (m, 1H), 7.75 (d, 1H), 7.81-7.88 (m, 2H), 7.96-8.00 (t, 1H), 8.04-8.10 (t, 2H), 8.40 (m, 1H), 8.43 (m, 1H), 8.75 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450308B2
Source datasetuspto-grants-2013_05
ORD IDord-0260a1349bd04eb1acec797029d013f0
Source noteuspto-grants-2013_05