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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2096402Generated: October 30, 2026

Ammonium iodide → HCID 58424333, compound

https://huagongshe.com/reaction/2096402

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium iodideHCID 25487—
ReactantEthanol, reaction products with ammonia, distn. residuesHCID 22020343—
ReactantHCID 58423912HCID 58423912—
ProductHCID 58424333HCID 5842433360%

Reaction Steps

A solution of 6-bromo-2-(2,3-difluorophenyl)-1′-methyl-2′-(methylthio) spiro[chroman-4,4′-imidazol]-5′(1′H)-one (63 mg, 0.14 mmol), NH4I (60.6 mg, 0.42 mmol) in a solution of NH3/EtOH (3 mL, 1.5 N) was heated at 110° C. in a tube under microwave reactor for 3 hrs. After cooling, the mixture was concentrated in vacuo to give the residue, which was purified by preparative TLC to afford 2′-amino-6-bromo-2-(2,3-difluorophenyl)-1′-methylspiro[chroman-4,4′-imidazol]-5′(1′H)-one (35 mg, 60%). 1H-NMR (CDCl3): 2.31 (d, 1H), 2.45 (t, 1H), 3.27 (s, 3H), 6.12 (d, 1H), 6.87 (m, 1H), 7.09 (m, 3H), 7.34 (m, 2H), 7.45 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450308B2
Source datasetuspto-grants-2013_05
ORD IDord-ad688322972242db8577ad12b362ad5d
Source noteuspto-grants-2013_05