HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1928816Generated: November 1, 2026
N,N-Dimethylglycine → HCID 57860963, compound
https://huagongshe.com/reaction/1928816
Participants
| Role | Name | HCID | Charge |
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| Reactant | N,N-Dimethylglycine | HCID 673 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| Reactant | Rac-n2-(8-methoxy-1,2,3,4-tetrahydro-naphthalen-1-yl)-quinoline-2,6-diamine | HCID 57860959 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57860963 | HCID 57860963 | 77.3% |
Reaction Steps
N,N-Dimethylglycine (49 mg, 0.48 mmol), N,N-diisopropyl ethyl amine (217 mg, 1.68 mmol) and 2-(1H-benzotriazole-1-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate (220 mg, 0.69 mmol) were dissolved in dichloromethane (6 mL) and dimethylformamide (1.5 mL). The reaction mixture was stirred at room temperature for 30 minutes. rac-N2-(8-Methoxy-1,2,3,4-tetrahydro-naphthalen-1-yl)-quinoline-2,6-diamine (150 mg, 0.47 mmol) was added and stirred was continued overnight. The reaction mixture was diluted with water and extracted with dichloromethane (3×). The combined organic phases were dried over sodium sulfate and evaporated. The crude product was purified by column chromatography (silica gel, dichloromethane/methanol 100:0→90:10). The title compound (147 mg, 77%) was obtained as a light brown solid; MS: m/e=405.5 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08183380B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-c2d72ed5172e4a05a975c22988ba767b |
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| Source note | uspto-grants-2012_05 |
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