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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1976139Generated: October 27, 2026

Diisopropylethylamine → HCID 22000409, compound

https://huagongshe.com/reaction/1976139

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Bromo-3,4-dihydro-2H-benzo[b]oxepin-5-oneHCID 13863234—
ReactantHCID 22254014HCID 22254014—
SolventEthanolHCID 702—
ProductHCID 22000409HCID 2200040965%

Reaction Steps

A solution containing benzyl N-(4-{[(aminocarbothioyl)amino]methyl}-cyclohexyl)carbamate (3.45 g, 10.73 mmol), 4-bromo-2,3,4,5-tetrahydro-1-benzoxepin-5-one (2.60 g, 10.78 mmol), and diisopropylethylamine (2.50 ml) in EtOH (50 ml) was heated at reflux for 4 hours. The solvent was removed and the residue was chromatographed on silica gel eluting with 1:3 EtOAc/hexane to yield 65% (3.2 g) of the product as a white solid: m.p. 124-127° C.; 1H-NMR (CDCl3) δ 1.09 (4H, pentet, J=10.4 Hz), 1.55 (1H, broad), 1.83 (2H, m), 2.04 (2H, broad), 3.10 (2H, t, J=6.2 Hz), 3.15 (2H, t, J=5.2 Hz), 3.43 (1H, broad) 4.33 (2H, t, J=5.2 Hz), 4.62 (1H, d, J=8.0 Hz), 5.08 (2H, s), 5.31 (1H, m), 7.00 (1H, dd, J=1.2 Hz, 7.8 Hz), 7.12 (2H, m), 7.35 (5H, s), 8.25 (1H, dd, J=1.7 Hz, 7.8 Hz). ESIMS m/z=464 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06225330B1
Source datasetuspto-grants-2001_05
ORD IDord-4367bc3546394c0d8251e0038eae7b7b
Source noteuspto-grants-2001_05