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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1927497Generated: November 3, 2026

Nitrogen → 4-Chloro-2-[4-(4-dimethylamino-benzyl)-piperazin-1-yl]-6-methyl-10,10-dioxo-10,11-dihydro-5-oxa-10lambda*6*-thia-dibenzo[a,d]cycloheptene-8-carboxylic acid methyl ester

https://huagongshe.com/reaction/1927497

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantBenzaldehyde, (dimethylamino)-HCID 34289—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant4-Chloro-6-methyl-10,10-dioxo-2-piperazin-1-yl-10,11-dihydro-5-oxa-10lambda*6*-thia-dibenzo[a,d]cyclo heptene-8-carboxylic acid methyl esterHCID 11541072—
CatalystTitanium isopropoxideHCID 11026—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product4-Chloro-2-[4-(4-dimethylamino-benzyl)-piperazin-1-yl]-6-methyl-10,10-dioxo-10,11-dihydro-5-oxa-10lambda*6*-thia-dibenzo[a,d]cycloheptene-8-carboxylic acid methyl esterHCID 131728479—

Reaction Steps

Titanium isopropoxide (0.33 mL. 1.09 mmol) was added to a solution of Example 104k (0.4 g, 0.91 mmol) and dimethylaminobenzaldehyde (0.136 g, 0.91 mmol) in dry methanol (10 mL). The reaction mixture was stirred at 50° C. in an atmosphere of N2 for 1.5 h. It was cooled, treated with sodium cyanoborohydride (0.054 g, 0.86 mmol) and stirred for 1.5 h. It was then treated with cold water and extracted with n-butanol. The organic layer was washed with water, brine, dried, concentrated and purified using flash chromatography (silica gel, MeOH/CHCl3) to obtain the title compound as a white solid. Yield: 0.275 g, (52.78%); 1H NMR (DMSO-d6): δ 2.7 (s, 3H, CH3), 3.00 (s, 6H, 2CH3), 3.20-3.25 (m, 4H, 2CH2), 3.55 (s, 4H, 2CH2), 3.95 (s, 3H, OCH3), 4.75 (s, 2H, CH2), 6.7-6.9 (m, 4H, Ar), 7.25 (s, 1H, Ar), 7.3 (s, 1H, Ar), 8.1 (s, 1H, Ar), 8.50 (s, 1H, Ar); MS: m/e (CI+) 570 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08183234B2
Source datasetuspto-grants-2012_05
ORD IDord-33912a08c888470d944eb7fc5138f269
Source noteuspto-grants-2012_05