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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1420747Generated: October 31, 2026

Pyridine → HCID 9912676, compound

https://huagongshe.com/reaction/1420747

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantHCID 57308558HCID 57308558—
ReactantHCID 178481946HCID 178481946—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 9912676HCID 991267621.2%

Reaction Steps

(3S,4S)-6-(4-tert-Butyldimethylsilyloxyphenyl)sulphonyl-3,4-dihydro-3,4-epoxy-2,2,3-trimethyl-2H-benzo[b]pyran (1.618 g) (see Preparation 14) and 2,3-dihydro-2-methyl-3-oxo-6-hydroxypyridazin (1.33 g) (see J.Org.Chem, 1971, 36, 3372) were suspended in dry 1,4-dioxane (15 ml), pyridine (0.275 ml) was added and the mixture was heated under reflux (a calcium chloride drying tube was attached to the flask) for 3 days. The solvent was removed under reduced pressure and the residue was partitioned between ethyl acetate and water. The organic phase was separated and dried (anhydrous sodium sulphate), the solvent was removed under reduced pressure and the crude product was chromatographed on silica using 1:99 methanol:ethyl acetate as the eluent to yield (3S,4R)-3,4-dihydro-4-(2,3-dihydro-2-methyl-3-oxopyridazin-6-yl)oxy-3-hydroxy-6-(4-hydroxyphenyl)sulphonyl-2,2,3-trimethyl-2H-benzo[b]pyran (0.352 g) as a white solid. Found: C,58.13; H,5.00; N,5.70. C23H24N2O7S requires C,58.46; H,5.12; N,5.93%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06071938
Source datasetuspto-grants-2000_06
ORD IDord-43fd5e09b0764f91a3a4b003bbb3e9db
Source noteuspto-grants-2000_06