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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2096473Generated: October 30, 2026

Ammonium iodide → HCID 58423892, compound

https://huagongshe.com/reaction/2096473

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium iodideHCID 25487—
ReactantEthanol, reaction products with ammonia, distn. residuesHCID 22020343—
ReactantHCID 58423942HCID 58423942—
ProductHCID 58423892HCID 5842389224%

Reaction Steps

A solution of 6-bromo-1′-(2-cyclopropylethyl)-2′-(2-cyclopropylethylthio)-2-phenylspiro[chroman-4,4′-imidazol]-5′(1′H)-one (40 mg, 0.076 mmol), and NH4I (22 mg, 0.153 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′-(2-cyclopropylethyl)-2-phenylspiro[chroman-4,4′-imidazol]-5′(1′H)-one (8 mg, 24%). 1H-NMR (MeOD): 0.01 (m, 2H), 0.34 (m, 2H), 0.61 (m, 1H), 1.48 (m, 2H), 2.10 (m, 1H), 2.37 (m, 1H), 3.67 (m, 2H), 5.12 (d, 0.3H), 5.74 (d, 0.7H), 6.70 (m, 1H), 7.00 (m, 1H), 7.31 (m, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450308B2
Source datasetuspto-grants-2013_05
ORD IDord-72271e0a3c264911ae23ffbe9e488c09
Source noteuspto-grants-2013_05