Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | HCID 57905300 | HCID 57905300 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 57904772 | HCID 57904772 | 100% |
Reaction Steps
To a solution of 5-benzyloxy-1-carboxymethoxy-6-oxo-3,7-diazatricyclo[7.2.2.02,7]trideca-2,4-diene-4-carboxylic acid ethyl ester (25 mg, 0.057 mmol) in DMF (1 mL) was added O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (HATU) (43 mg, 0.11 mmol) and 4-(dimethylamino)pyridine (DMAP) (14 mg, 0.11 mmol) and the mixture stirred at room temperature for 15 min under N2. To this was added a 2M THF solution of dimethylamine (0.057 mL, 0.11 mmol) and the mixture stirred at room temperature for 90 min. The mixture was concentrated and the residue taken up in ethyl acetate (10 mL), washed with 1N HCl followed by brine, then dried (Na2SO4) and concentrated to provide the title compound (36 mg, 0.057 mmol, 100% yield) as a crude amber film: HPLC: retention time=2.15 min; LCMS: m/z 470 (M+H); 1H NMR (400 MHz, CDCl3) δ ppm 1.23 (3H, t, J=6.6 Hz), 1.65-1.76 (2H, m), 1.88-2.01 (2H, m), 2.11-2.26 (4H, m), 2.46 (1H, brs), 2.90 (3H, s), 2.95 (3H, s), 4.10 (2H, t, J=7.0 Hz), 4.23-4.33 (4H, m), 5.24 (2H, s), 7.27-7.38 (3H, m), 7.46 (2H, d, J=7.0 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08129398B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-7c7938bab8d0475fa0d287e1eef247dc |
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| Source note | uspto-grants-2012_03 |
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