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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1453258Generated: October 26, 2026

3-Chloro-6-ethyl-4-hydroxy-6-methyl-5,6-dihydro-pyran-2-one → 3-(5-Chloro-1-isopropyl-1H-benzoimidazol-2-ylsulfanyl)-6-ethyl-4-hydroxy-6-methyl-5,6-dihydro-pyran-2-one

https://huagongshe.com/reaction/1453258

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-6-ethyl-4-hydroxy-6-methyl-5,6-dihydro-pyran-2-oneHCID 58762455—
ReactantHCID 178456613HCID 178456613—
Product3-(5-Chloro-1-isopropyl-1H-benzoimidazol-2-ylsulfanyl)-6-ethyl-4-hydroxy-6-methyl-5,6-dihydro-pyran-2-oneHCID 58762295—

Reaction Steps

The title compound was prepared from 3-Chloro-6-ethyl-4-hydroxy-6-methyl-5,6-dihydro-pyran-2-one (from Step 1) and 5-Chloro-1-isopropyl-1H-benzoimidazole-2-thiol using the coupling method described in Example C(4). 1H NMR (CDCl3): δ 0.95 (t, 3H, J=7.5 Hz), 1.41 (s, 3H), 1.68 (d, 6H, J=7.0 Hz), 1.75 (m, 2H), 2.52 (d, 1H, J=17.1 Hz), 2.74 (d, 1H, J=17.1 Hz), 6.97 (m, 1H), 6.56 (br s, 1H), 7.28 (d, 1H, J=8.9 Hz), 7.48 (d, 1H, J=8.9 Hz), 7.60 (s, 1H). Anal. Calcd. For C18H21N2O3SCl.0.1H2O: C, 56.49; H, 5.58; N, 7.32. Found: C, 56.32; H, 5.56; N, 7.17.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07473790B2
Source datasetuspto-grants-2009_01
ORD IDord-71ac5a3ba9e041479ad12c4e26313988
Source noteuspto-grants-2009_01