HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 13659Generated: October 26, 2026
Morpholine → 6-Bromo-3-methanesulfonyl-2-methyl-4-morpholin-4-yl-quinoline
https://huagongshe.com/reaction/13659
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 6-Bromo-4-chloro-3-methanesulfonyl-2-methyl-quinoline | HCID 12001623 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-Bromo-3-methanesulfonyl-2-methyl-4-morpholin-4-yl-quinoline | HCID 12001810 | 81.5% |
Reaction Steps
6-Bromo-4-chloro-3-methanesulfonyl-2-methyl-quinoline (compound of example D.1) (11.5 g, 34.4 mmol), morpholine (3.3 mL, 37.8 mmol) and N,N-diisopropyl ethyl amine (6.5 mL, 37.8 mmol) were heated at 100° C. in dry N,N-dimethylformamide (10 mL) for 30 min. The reaction mixture was evaporated to dryness, and the residue extracted with dichloromethane, 10% Na2CO3 and sat. NaCl. The crude product was stirred and heated at 80° C. in ethyl acetate (80 mL) for 10 min, the resulting suspension was cooled in ice, the crystals were filtered off and washed with little cold ethyl acetate. One obtained 10.8 g (81%) of white crystals. MS: m/z=385/387 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07728142B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-d229c40c67a643efaf5942647d32a488 |
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| Source note | uspto-grants-2010_06 |
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