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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1979059Generated: October 29, 2026

HCID 11149822, compound → HCID 18331717, compound

https://huagongshe.com/reaction/1979059

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 11149822HCID 11149822—
ReactantHCID 11242609HCID 11242609—
ReactantHCID 11437086HCID 11437086—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
ProductHCID 18331717HCID 1833171770%

Reaction Steps

2.06 g (7.72 mmol) of the mixture of 3-isopropoxycarbonylamino-{2-(E)-(4-methyl-2-penten-2-yl)}thiophene, 3-isopropoxycarbonylamino-{2-(Z)-(4-methyl-2-penten-2-yl)}thiophene, and 3-isopropoxycarbonylamino-{2-(4-methyl-1-penten-2-yl) }thiophene obtained in Example 13 and 0.41 g of 5% palladium carbon (Degussa chemical catalyst E106R/W) were charged into 20 ml of methanol, and after nitrogen purge, a hydrogenation reaction was conducted at normal pressure under hydrogen atmosphere for 9 hours. After nitrogen purge, the catalyst was filtrated off, and the solvent was distilled off under reduced pressure. The resulting residue was purified by silica gel column chromatography (eluent: hexane/ethyl acetate=9/1) to obtain 1.61 g of the intended compound as a colorless crystal (yield: 70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06239282B1
Source datasetuspto-grants-2001_05
ORD IDord-14c1bd2cbd79493699d505f09651e037
Source noteuspto-grants-2001_05