HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methylmorpholine → Methyl 3(6-Hexanamido-2,3-dihydrobenz-1,4-oxazin-4-ylmethyl)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Hexanoyl chloride | HCID 67340 | — |
| Reactant | Methyl 3-(6-amino-2,3-dihydrobenz-1,4-oxazin-4-ylmethyl)benzoate | HCID 54048005 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 3(6-Hexanamido-2,3-dihydrobenz-1,4-oxazin-4-ylmethyl)benzoate | HCID 23365863 | — |
Reaction Steps
Hexanoyl chloride (0.135 g.) was added dropwise to a stirred solution of methyl 3-(6-amino-2,3-dihydrobenz-1,4-oxazin-4-ylmethyl)benzoate (X) (0.3 g.), and N-methylmorpholine (0.101 g.) in dichloromethane (30 ml.). After 0.5 hours, the mixture was diluted with dichloromethane, washed with water, dried (MgSO4) and evaporated to give an oil which was filtered through a short column of silica gel using 35:65 v/v ethyl acetate:hexane to give the title compound as a syrup; partial NMR (80 MHz, CDCl3): 0.8-1.9[complex m,9H, CH3 (CH2)3 ]; 2.2(m,2H, CH2CONH); 3.3(m,2H, N.CH2.CH2.O); 3.9(s,3H, OMe); 4.2(m,2H, N.CH2.CH2O); 4.5(s,2H, N.CH2Ar).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05391758 |
| Source dataset | uspto-grants-1995_02 |
| ORD ID | ord-940e3e8fb104414d86d66104cb41bc3a |
| Source note | uspto-grants-1995_02 |