HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 422225Generated: October 30, 2026
Dimethyl Sulfoxide → HCID 59750672, compound
https://huagongshe.com/reaction/422225
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 59750648 | HCID 59750648 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59750672 | HCID 59750672 | 86.2% |
Reaction Steps
Combine DCM (3 mL) and oxalyl chloride (41 uL) under nitrogen atmosphere at −78° C., and then add DMSO (49 uL) in DCM (2 mL). After the solution stirs for 15 minutes, add 6-(2-Hydroxymethyl-indan-5-yloxy)nicotinamide (33.1 mg, 0.116 mmol) in DCM (2 mL). After 15 minutes, add Et3N (97 uL, 0.70 mmol). After the reaction gradually warms to room temperature over the next 5 hours, then quench with water. Add the mixture to a separatory funnel and extract the product with DCM. Wash the organic phase with brine and then dry over Na2SO4. After concentrating under reduced pressure, flash chromatograph using 10% THF/CH2Cl2 eluent affords 27.4 mg, 0.10 mmol (84% yield) of the title compound: 1H NMR (500 MHz, CDCl3); 3.1-3.2 (2H, m), 3.2-3.4 (3H, m), 6.8-7.0 (4H, m), 7.1-7.3 (1H, m), 8.8-8.9 (1H, m), 8.4 (1H, s), 9.7 (1H, s); TLC 1:6 THF:CH2Cl2Rf:=0.7.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08101638B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-0c37be6732e94f8b9b0ec379a0cbae44 |
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| Source note | uspto-grants-2012_01 |
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