Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1255455Generated: October 31, 2026

8-Chloro-1-(4-oxo-cyclohexyl)-4H,6H-2,3,5,10b-tetraaza-benzo[e]azulene-5-carboxylic acid tert-butyl ester → 8-Chloro-1-(4-hydroxy-4-o-tolyl-cyclohexyl)-4H,6H-2,3,5,10b-tetraaza-benzo[e]azulene-5-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1255455

Reaction equation

Participants

RoleNameHCIDCharge
Reactant8-Chloro-1-(4-oxo-cyclohexyl)-4H,6H-2,3,5,10b-tetraaza-benzo[e]azulene-5-carboxylic acid tert-butyl esterHCID 58458742—
ReactantHCID 178424304HCID 178424304—
SolventTetrahydrofuranHCID 8028—
Product8-Chloro-1-(4-hydroxy-4-o-tolyl-cyclohexyl)-4H,6H-2,3,5,10b-tetraaza-benzo[e]azulene-5-carboxylic acid tert-butyl esterHCID 5845873670%

Reaction Steps

To a solution of 8-chloro-1-(4-oxo-cyclohexyl)-4H,6H-2,3,5,10b-tetraaza-benzo[e]azulene-5-carboxylic acid tert-butyl ester (0.2 g, 0.5 mmol) in dry tetrahydrofuran (5 ml) was added a 1M o-tolylmagnesium chloride solution in tetrahydrofuran (0.5 ml, 0.5 mmol) at room temperature. After stirring for 2 h the reaction mixture was quenched with aqueous saturated ammonium chloride solution and extracted with two portions of ethyl acetate. The combined organic layers were washed with one portion of brine, dried over anhydrous sodium sulfate and concentrated in vacuo. Flash-chromatography with n-heptane/ethyl acetate as eluent gave the title compound (0.17 g, 70%) as white solid. MS m/e: 509 ([[M+H]]+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461151B2
Source datasetuspto-grants-2013_06
ORD IDord-84406677a40b4b55a69c8a103b306231
Source noteuspto-grants-2013_06