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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2096449Generated: October 29, 2026

Ammonium iodide → 2'-amino-6-bromo-1'-methyl-2-phenylspiro[chroman-4,4'-imidazol]-5'(1'H)-one

https://huagongshe.com/reaction/2096449

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium iodideHCID 25487—
ReactantEthanol, reaction products with ammonia, distn. residuesHCID 22020343—
ReactantHCID 58423832HCID 58423832—
Product2'-amino-6-bromo-1'-methyl-2-phenylspiro[chroman-4,4'-imidazol]-5'(1'H)-oneHCID 5842376838.3%

Reaction Steps

A solution of 6-bromo-1′-methyl-2′-(methylthio)-2-phenylspiro[chroman-4,4′-imidazol]-5′(1′H)-one (59 mg, 0.142 mmol), NH4I (41.5 mg, 0.286 mmol) in a solution of NH3/EtOH (4 mL, 1.5 N) was heated at 110° C. in a tube in a microwave reactor for 2-2.5 h. After cooling, the mixture was concentrated in vacuo to give a residue, which was purified by preparative TLC to afford 2′-amino-6-bromo-1′-methyl-2-phenylspiro[chroman-4,4′-imidazol]-5′(1′H)-one (21 mg, 38%). 1H-NMR (MeOD): 2.04 (d, 1H), 2.15 (dd, 1H), 4.51 (m, 1H), 5.75 (d, 1H), 6.78 (m, 1H), 6.99 (d, 1H), 7.20-7.26 (m, 2H), 7.26-7.35 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450308B2
Source datasetuspto-grants-2013_05
ORD IDord-8844646ace904ca5ab88b081451291e6
Source noteuspto-grants-2013_05