Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetaldehyde | HCID 177 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 67457633 | HCID 67457633 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 46830971 | HCID 46830971 | 63% |
Reaction Steps
N-(4-Methyl-3-[(4-pyridin-3-ylpyrimidin-2-yl)amino]phenyl)-1-piperazin-1-yl-2,3-dihydro-1H-indene-5-carboxamide tetrahydrochloride (100 mg, 0.15 mmol) was dissolved in DMF (2 mL) and triethylamine (101 mg, 1 mmol) was added followed by acetaldehyde (26 mg, 0.6 mmol). After the solution was stirred for 20 minutes, sodium triacetoxyborohydride (128 mg, 0.6 mmol) was added. The solution obtained was stirred overnight at room temperature and then purified by high performance liquid chromatography at pH=10 to obtain 50 mg (63% yield) of the title compound. MS (M+1)=523.29. 1HNMR (DMSO-d6, ppm): δ 10.14 (s, 1H); 9.25 (s, 1H); 8.98 (s, 1H); 8.67 (d, J=4.8 Hz, 1H); 8.49 (d, J=5.2 Hz, 1H); 8.46 (d, J=8.6 Hz, 1H); 8.05 (s, 1H); 7.77 (s, 1H); 7.75 (d, J=8.8 Hz, 1H); 7.50 (dd, J=8.0 Hz, 4.8 Hz, 1H); 7.46 (d, J=8.2 Hz, 1H); 7.41 (d, J=5.2 Hz, 1H); 7.35 (d, J=7.6 Hz, 1H); 7.17 (d, J=8.8 Hz, 1H); 4.31 (t, J=6.8 Hz, 1H); 2.2-3.0 (m, 12H); 2.20 (s, 3H); 2.03 (m, 2H); 0.95 (t, J=7.0 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08703771B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-2620d035200a4fdaa91bf4fc2058c5a7 |
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| Source note | uspto-grants-2014_04 |
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