Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-Oxo-1-pyrrolidinepropanoic acid | HCID 3146688 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Product | HCID 24883123 | HCID 24883123 | 49% |
Reaction Steps
To a solution of (3aS,7aS)-1-(1,4′-bipiperidin-4-yl)-3-methyloctahydro-2H-benzimidazol-2-one. 2HCl (71 mg, 0.18 mmol) in DMF (4 mL) was added diisopropylethylamine (0.1 mL, 0.57 mmol) and 3-(2-oxopyrrolidin-1-yl)propanoic acid (34 mg, 0.2 mmol) at room temperature, the mixture was sonicated to dissolve the starting materials and HATU (75 mg, 0.2 mmol) was then added. The solvent was removed under reduced pressure and the mixture was diluted in dichloromethane (60 mL). The mixture was washed with 1N NaOH (5 mL) and brine (5 mL) and concentrated in vacuo. The residue was then purified by high pH prep LCMS to provide the title compound as a white solid (44 mg, 49%). HCl salt-1H NMR (400 MHz, METHANOL-D4) δ ppm 1.24-1.53 (m, 4H), 1.53-1.71 (m, 1H), 1.76-2.11 (m, 7H), 2.10-2.37 (m, 4H), 2.41 (t, J=8.20 Hz, 3H), 2.55-2.81 (m, 4H), 2.66 (s, 3H), 2.87-3.01 (m, 1H), 3.05-3.22 (m, 3H), 3.39-3.67 (m, 8H), 3.74-3.89 (m, 1H), 4.14 (d, J=14.45 Hz, 1H), 4.67 (d, J=13.67 Hz, 1H). MS (M+1): 460.2
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07956069B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-a4e7de5270704e4b88f011561db07bfd |
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| Source note | uspto-grants-2011_06 |
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