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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2258145Generated: November 1, 2026

HCID 22915344, compound → HCID 22915337, compound

https://huagongshe.com/reaction/2258145

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22915344HCID 22915344—
ReactantHCID 22915349HCID 22915349—
ProductHCID 22915337HCID 22915337—

Reaction Steps

As shown in FIG. 24, the synthesis pathway for the compounds of the present invention involves starting with the following compound, Compound 1: ##STR5## This starting compound in the synthesis of Compound 2 is 4,5'-dimethyl-8-methoxypsoralen. The synthesis of this precursor compound has been described previously in the literature. See Bender, et al., J. Org. Chem. 44:2176 (1979). Alternatively, the starting compound may be synthesized by the following method: 8-acetyl-7-(2-chloroallyl)oxy-4-methylcoumarin, described in Bender, et al, J. Org. Chem. 48:2709 (1983), is initially oxidized to a phenolic compound, 7-(2-chloro-2-propenyl)oxy-8-hydroxy-4-methylcoumarin, and then methylated, providing 7-(2-chloro-2-propenyl)oxy-8-methoxy-4-methylcoumarin. Claisen rearrangement provides 6-(2-chloro-2-propenyl)-7-hydroxy-8-methoxy-4-methylcoumarin, which is then converted to 4,5'-dimethyl-8-methoxypsoralen.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05659050
Source datasetuspto-grants-1997_08
ORD IDord-56c3cf93a19a474ea298b262ca4e7c4b
Source noteuspto-grants-1997_08