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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1173375Generated: November 1, 2026

Dimethyl Sulfoxide → HCID 11640089, compound

https://huagongshe.com/reaction/1173375

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 131728531HCID 131728531—
SolventDichloromethaneHCID 6344—
ProductHCID 11640089HCID 11640089—

Reaction Conditions

Temperature22 °C

Reaction Steps

DMSO (2.6 mL, 37.5 mmol) was added at −70° C. to a solution of oxalyl chloride (0.46 mL, 37.5 mmol) in dichloromethane (10 mL). Reaction mixture was stirred for 5 minutes and to this (4-chloro-6-methyl-10,10-dioxo-2-piperazin-1-yl-10,11-dihydro-5-oxa-10lambda*6*-thia-dibenzo[a,d]-cyclohepten-8-yl)-methanol (0.489 g, 1.19 mmol) [obtained by following the procedure described in Example 34] in dichloromethane (5 mL) was added. Reaction mixture was stirred for 5 minutes and to this triethylamine (8.4 mL, 62.5 mmol) was added. Reaction mixture was warmed to room temperature (22° C.) and stirred for 0.5 h. the reaction mixture was diluted with dichloromethane (200 mL), washed with water (100 mL), brine (50 mL) and dried over sodium sulphate. The crude product obtained was purified by column chromatography (silica gel, ethylacetate-pet ether) to obtain the title compound. Yield: 0.2 g (42%); 1H NMR (DMSO-d6, 300 MHz): δ 2.64 (s, 3H, CH3), 3.20 (s, 4H, 2CH2), 3.20 (s, 4H, 2CH2), 5.15 (s, 2H, CH2), 7.14 (d, 2H, Ar), 8.03 (s, 1H, Ar), 8.24 (s, 1H, Ar), 9.97 (s, 1H, CHO); MS: m/e (EI) 406 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834052B2
Source datasetuspto-grants-2010_11
ORD IDord-fb0515a55218402fa667afc542b289eb
Source noteuspto-grants-2010_11