HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 426012Generated: October 31, 2026
1,1-Dichloroethane → HCID 66703839, compound
https://huagongshe.com/reaction/426012
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,1-Dichloroethane | HCID 6365 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | 7-amino-1-methyl-3,4-dihydroquinolin-2(1H)-one | HCID 33699394 | — |
| Reactant | HCID 66703628 | HCID 66703628 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 66703839 | HCID 66703839 | — |
Reaction Steps
HATU (220 mg) and triethylamine (0.08 mL) were added to a dichloroethane (10 mL) solution of 4-tert-butyl-2-{[(1S,2S)-2-pyrrolidin-1-ylcyclohexyl]amino}benzoic acid (200 mg) and 7-amino-1-methyl-3,4-dihydroquinolin-2(1H)-one (102 mg), followed by stirring at room temperature for 12 hours. A 1 M sodium hydroxide aqueous solution was added to the reaction liquid, followed by extraction with chloroform. After drying of the organic layer, the solution was concentrated under a reduced pressure and the resulting residue was purified by silica gel column chromatography (chloroform:methanol, 95:5). By adding fumaric acid (22 mg) to an ethyl acetate solution of the resulting free base, 4-tert-butyl-N-(1-methyl-2-oxo-1,2,3,4-tetrahydroquinolin-7-yl)-2-{[(1S,2S)-2-pyrrolidin-1-ylcyclohexyl]amino}benzamide fumarate (190 mg) was obtained as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08106190B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-1522f7c5049f4afd8a99b834256b9ffd |
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| Source note | uspto-grants-2012_01 |
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