HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1641057Generated: November 4, 2026
Methyl(2-phenoxyethyl)amine → ethyl 2-(4-acetyl-3,4-dihydro-2H-benzo[b][1,4]oxazin-6-yl)-5-(methyl(2-phenoxyethyl)amino)thiazole-4-carboxylate
https://huagongshe.com/reaction/1641057
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl(2-phenoxyethyl)amine | HCID 37732 | — |
| Reactant | ethyl 2-(4-acetyl-3,4-dihydro-2H-benzo[b][1,4]oxazin-6-yl)-5-chlorothiazole-4-carboxylate | HCID 59418731 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | ethyl 2-(4-acetyl-3,4-dihydro-2H-benzo[b][1,4]oxazin-6-yl)-5-(methyl(2-phenoxyethyl)amino)thiazole-4-carboxylate | HCID 59418712 | 52% |
Reaction Steps
To ethyl 2-(4-acetyl-3,4-dihydro-2H-benzo[b][1,4]oxazin-6-yl)-5-chlorothiazole-4-carboxylate (7D) (0.15 g, 0.41 mmol) and methyl-(2-phenoxy-ethyl)-amine (1.24 g, 8.1 mmol) was added DMF (10 mL). The reaction mixture was allowed to heat to 70° C. for 48 hours. The reaction mixture was cooled to rt and concentrated under reduced pressure. The crude residue was purified by column chromatography on silica gel eluting with a gradient of 0 to 80% EtOAc in hexanes to provide 0.102 g (52%) of the desired product ethyl 2-(4-acetyl-3,4-dihydro-2H-benzo[b][1,4]oxazin-6-yl)-5-(methyl(2-phenoxyethyl)amino)thiazole-4-carboxylate (20A): LC/MS (APCI): m/z 482.1 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08114893B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-f368d8eb801d428ca5b4c1b49649c535 |
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| Source note | uspto-grants-2012_02 |
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