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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1408707Generated: October 31, 2026

N-methylhydroxylamine hydrochloride → 6-bromo-2'methyl-2-phenyl-2'H-spiro(chroman-4,5'-(1,2,4)oxadiazol)-3'-amine

https://huagongshe.com/reaction/1408707

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-methylhydroxylamine hydrochlorideHCID 77906—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 178511903HCID 178511903—
SolventMethanolHCID 887—
Product6-bromo-2'methyl-2-phenyl-2'H-spiro(chroman-4,5'-(1,2,4)oxadiazol)-3'-amineHCID 5842378696.8%

Reaction Steps

To a solution of methylhydroxylamine HCl salt (26 mg, 0.307 mmol) in anhydrous MeOH (10 mL) was added NaOMe (25 wt. % in MeOH, 0.07 mL, 0.276 mmol), followed by (Z)—N-(6-bromo-2-phenylchroman-4-ylidene)cyanamide (100 mg, 0.307 mmol). After stirring for 10 minutes, the solvent was removed in vacuo. The residue was dissolved in DCM (20 mL). The mixture was filtered, and the solvent was removed in vacuo to give 6-bromo-2′methyl-2-phenyl-2′H-spiro(chroman-4,5′-(1,2,4)oxadiazol)-3′-amine (100 mg, 87%), which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921359B2
Source datasetuspto-grants-2014_12
ORD IDord-82c52faf824d4d19a7117381255975a5
Source noteuspto-grants-2014_12