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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443573Generated: October 29, 2026

HCID 23467841, compound → HCID 23467839, compound

https://huagongshe.com/reaction/443573

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 23467841HCID 23467841—
ReactantHCID 178418361HCID 178418361—
ProductHCID 23467839HCID 23467839—

Reaction Steps

Catalytic hydrogenation of 3-cyclopropylmethyl 9-methoxy-2,3-dihydro-1H-benzo[4,5]furo[3,2-e]isoquinolin-4[4H]-one (Example 4c) is carried out as in Example 4d but the reaction is stopped after one mole equivalent of hydrogen has been taken up, giving 3-cyclopropylmethyl-9-methoxy-2,6,7,7a-tetrahydro-1H-benzo[4,5]furo[3,2-e]isoquinolin-4[3H]-one. This, on treatment with m-chloroperbenzoic acid gives 3-cyclopropylmethyl-4a,5-epoxy-9-methoxy-2,4a,5,6,7,7a-hexahydro-1H-benzo[4,5]furo[3,2-e]isoquinolin-4[3H]-one which is reduced with lithium aluminum hydride to 3-cyclopropylmethyl-9-methoxy-2,3,4,4a,5,6,7,7a-octahydro-1H-benzo[4,5]furo[3,2-e]isoquinolin-4a-ol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04260761
Source datasetuspto-grants-1981_04
ORD IDord-7b23ab1bb1c64eb7917180b5e103e9ce
Source noteuspto-grants-1981_04