HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2425106Generated: October 28, 2026
Dimethyl Sulfoxide → HCID 11640089, compound
https://huagongshe.com/reaction/2425106
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 131728531 | HCID 131728531 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 11640089 | HCID 11640089 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07964631B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-4f8c5da3d6044103a42679b568255102 |
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| Source note | uspto-grants-2011_06 |
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