HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1669935Generated: October 29, 2026
N,N-Dimethylethylenediamine → HCID 57448661, compound
https://huagongshe.com/reaction/1669935
Participants
| Role | Name | HCID | Charge |
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| Reactant | N,N-Dimethylethylenediamine | HCID 66053 | — |
| Reactant | HCID 16045611 | HCID 16045611 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 57448661 | HCID 57448661 | 19.1% |
Reaction Steps
6-chloro-N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)-pyridine-3-sulfonamide (100 mg, 0.21 mmol), prepared using procedures similar to those used in Example 8, KHCO3 (40 mg, 0.40 mmol), N1,N1-dimethylethane-1,2-diamine (225 μL, 2.0 mmol) and dry DMF (1.0 mL) were combined and heated to 130° C. with stirring overnight. The reaction mixture was concentrated in vacuo and purified by preparative HPLC to give N-(3-(3,5-dimethoxy-phenylamino)-quinoxalin-2-yl)-6-(2-(dimethylamino)ethylamino)pyridine-3-sulfonamide (21.0 mg, 19%). 1H NMR (400 MHz, DMSO-d6) δ 8.76 (br s, 1H), 8.63 (d, 1H), 8.07 (dd, 1H), 7.40 (m, 1H), 7.34 (m, 1H), 7.28 (d, 2H), 7.14 (m, 4H), 6.47 (d, 1H), 6.12 (m, 1H), 3.75 (s, 6H), 3.35 (m, 2H), 3.14 (m, 2H), 2.74 (s, 6H). MS (EI) m/z for C25H29N7O4S: 524.1 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07989622B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-fe1fcddf351f40a185aff30b804cdd1d |
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| Source note | uspto-grants-2011_08 |
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