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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2275305Generated: October 31, 2026

7-Methoxy-1,1-dimethyl-3,4-dihydronaphthalen-2(1H)-one → HCID 66835214, compound

https://huagongshe.com/reaction/2275305

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-Methoxy-1,1-dimethyl-3,4-dihydronaphthalen-2(1H)-oneHCID 13011007—
Reactant2-Bromo-5-chlorophenolHCID 13284272—
Reactant8-Hydroxy-6,6-dimethyl-11-oxo-6,11-dihydro-5H-benzo[b]carbazole-3-carbonitrileHCID 66833861—
ProductHCID 66835214HCID 66835214—

Reaction Steps

The compounds described in the following Table 43 were synthesized according to the method shown below. According to the method used for the preparation of Compound Z10, Z11 and Z12, 3-chloro-8-methoxy-6H-benzo[b]naphtho[2,3-d]furan-11-one was prepared from Compound A2 and 2-bromo-5-chlorophenol. Subsequently, demethylation was carried out according to the method that is used for the preparation of Compound A6, and thus 3-chloro-8-hydroxy-6H-benzo[b]naphtho[2,3-d]furan-11-one was obtained. Thereafter, according to Mitsunobu reaction that is used for the preparation of Compound A7-1 or the alkylation method that is used for the preparation of A7-17, a corresponding side chain was introduced and, if necessary, functional group modification such as deprotection, etc. was carried out to prepare the compounds listed below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126931B2
Source datasetuspto-grants-2015_09
ORD IDord-33357b03a92f4cd88f170f0fe630090b
Source noteuspto-grants-2015_09