Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | HCID 59201687 | HCID 59201687 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59201718 | HCID 59201718 | — |
Reaction Steps
Crude (2S,3S)-3-cyclohexyl-2-(1,3-dioxoisoindolin-2-yl)-3-hydroxypropanal (3.22 g, 10.7 mmol, calculated according to theoretical yield) was dissolved in anhydrous THF (20 mL). The solution was cooled to 0° C. Acetic acid (5.5 mL, 90 mmol), methylamine solution (33% in EtOH, 5.0 mL, 40.0 mmol) and NaHB(OAc)3 (8.80 g, 40.0 mmol) were added sequentially and in single portions. The ice bath was removed and the mixture was stirred for 2 h at rt. The solvent was stripped and the crude 2-((1S,2R)-1-cyclohexyl-1-hydroxy-3-(methylamino)propan-2-yl)isoindoline-1,3-dione (6.45 g) was used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08487108B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-ef344ac9e56340b5ac101edd2c3b4c91 |
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| Source note | uspto-grants-2013_07 |
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