Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 59441879 | HCID 59441879 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178486469 | HCID 178486469 | 81% |
Reaction Steps
A solution of of 2-({2-{[1-acetyl-5-(methyloxy)-2,3-dihydro-1H-indol-6-yl]amino}-7-[(4-methylphenyl)sulfonyl]-7H-pyrrolo[2,3-d]pyrimidin-4-yl}amino)-6-fluorobenzamide (104 mg, 0.17 mmol) in methanol (10 mL) and THF (20 mL) was treated with a solution of sodium methoxide (0.5M in MeOH, 3.3 mL, 1.7 mmol). The resulting mixture was stirred at rt for 2 days, then diluted with EtOAc (100 mL) and a saturated NaCl solution. The organic layer was washed with a saturated NaHCO3 solution, concentrated onto Celite and purified by silica gel chromatography using 0-5% MeOH (containing 0.2% NH3)/CH2Cl2 to obtain 2-[(2-{[1-acetyl-5-(methyloxy)-2,3-dihydro-1H-indol-6-yl]amino}-1H-pyrrolo[2,3-d]pyrimidin-4-yl)amino]-6-fluorobenzamide as a yellow solid (63 mg, 81%). 1H NMR (400 MHz, DMSO-d6) δ ppm 2.13 (s, 3H), 3.09-3.19 (m, 2H), 3.78 (s, 3H), 4.06-4.15 (m, 2H), 6.23 (s, 1H), 6.88 (J=9.71 Hz, 9.34 Hz, 1H), 6.95 (s, 2H), 7.27-7.37 (m, 1H), 7.58 (s, 1H), 8.02 (s, 1H), 8.10 (s, 1H), 8.50 (d, J=8.42 Hz, 1H), 8.62 (s, 1H), 10.52 (s, 1H), 11.29 (s, 1H); ESIMS (M+H)+=475.99.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07981903B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-390a0689dacc4f5cae4faaf397c60623 |
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| Source note | uspto-grants-2011_07 |
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