HuagongsheHuagongshe Chemistry Print Report · For research reference only
Morpholine → (R)-N-Boc-1-morpholino-2-propanamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | (R)-2-((tert-butoxycarbonyl)amino)propyl methanesulfonate | HCID 14427185 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (R)-N-Boc-1-morpholino-2-propanamine | HCID 57851166 | 62% |
Reaction Steps
Heat a mixture of (R)-methanesulfonic acid 2-tert-butoxycarbonylamino-propyl ester (0.083 mol, 20 g) and morpholine (0.83 mol, 72.2 g) in acetonitrile (210 mL) to 65° C. for 16 h. Concentrate the reaction mixture, dilute the residue with water, extract with dichloromethane, combine organic layer and wash with water. Dry the organic layer over anhydrous sodium sulfate, filter and concentrate under vacuum to obtain the title compound (12 g, 62%) as yellow thick oil. 1H NMR (400 MHz, CDCl3) δ 1.13 (d, 3H), 1.43 (s, 9H), 2.21 (dd, 1H), 2.26-2.32 (m, 1H), 2.35-2.39 (m, 2H), 2.48-2.55 (m, 2H), 3.63-3.70 (m, 5H), 4.68 (br s, 1H, —NH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07994164B2 |
| Source dataset | uspto-grants-2011_08 |
| ORD ID | ord-cc610e987b104c01af76fa9e030e6186 |
| Source note | uspto-grants-2011_08 |