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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 505770Generated: November 4, 2026

4-Methoxybenzyl alcohol → (+/-)-(3SR,3aRS)-4-methoxybenzyl 2-(3-chloro-4-cyanophenyl)-3-cyclopentyl-3,3a,4,5-tetrahydro-2H-benzo[g]indazole-7-carboxylate

https://huagongshe.com/reaction/505770

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxybenzyl alcoholHCID 7738—
Reactant(+/-)(3SR,3aRS)-2-(3-chloro-4-cyanophenyl)-3-cyclopentyl-3,3a,4,5-tetrahydro-2H-benzo[g]indazole-7-carboxylic acidHCID 24983760—
Product(+/-)-(3SR,3aRS)-4-methoxybenzyl 2-(3-chloro-4-cyanophenyl)-3-cyclopentyl-3,3a,4,5-tetrahydro-2H-benzo[g]indazole-7-carboxylateHCID 68799770—

Reaction Steps

The title compound was prepared according to Method E from (±)-(3SR,3aRS)-2-(3-chloro-4-cyanophenyl)-3-cyclopentyl-3,3a,4,5-tetrahydro-2H-benzo[g]indazole-7-carboxylic acid, Example 15 and p-methoxybenzyl alcohol. Yellow solid, 194 mg. ES-MS m/z 540 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07781428B2
Source datasetuspto-grants-2010_08
ORD IDord-368d9241805c41dea137a7b92bca4e06
Source noteuspto-grants-2010_08