Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 24996234 | HCID 24996234 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 59785882 | HCID 59785882 | — |
Reaction Steps
To the product of Example 1 (500 mg, 1.155 mmol) was added paraformaldehyde (347 mL, 11.6 mmol) and pyrrolidine (0.243 mL, 2.94 mmol) in EtOH (10 mL)/THF (3 mL). The reaction vessel was sealed and heated to 65° C. for 4.5 h. The reaction was cooled and diluted with EtOAc and washed with brine. The solution was dried (Na2SO4) and concentrated. The residue was dissolved in THF (8 mL) and MeOH (1 mL) and NaBH4 (87 mg, 2.31 mmol) was added. After 25 min the reaction was diluted with EtOAc and washed with 2 M aq HCl and brine. The concentrated residue was purified by flash chromatography on silica gel gradient eluted with 0-60% EtOAc in hexane affording the title compound. (LC-2) HPLC/MS: 448.2 (M+1), 450.2 (M+3); Rt=4.23 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07999107B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-7edb59d14280493db58497a4d7bcb2fc |
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| Source note | uspto-grants-2011_08 |
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