Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 68913128 | HCID 68913128 | — |
| Reactant | HCID 178418332 | HCID 178418332 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57829801 | HCID 57829801 | 100% |
Reaction Steps
A solution of ({2-[3-methoxy-4-(4-methyl-imidazol-1-yl)-phenylamino]-6-methyl-pyrimidin-4-yl}-methyl-amino)-acetic acid benzyl ester (32 mg, 0.07 mmol) in 2 mL of tetrahydrofurane was cooled in an ice-bath and treated with a 3 molar solution of methyl magnesium chloride in tetrahydrofurane (0.15 mL, 1.5 mmol). The mixture was stirred for 10 minutes in the ice-bath and for additional 2 hours at 20° C. Hydrolysis and extraction with ethyl acetate gave the title compound as a yellowish sticky gum (27 mg, 100%). MS ISP (m/e): 397.3 (100) [(M+H)+]. 1H NMR (CDCl3, 300 MHz): δ (ppm)=7.62 (s, 1H), 7.52 (s, 1H), 7.37 (d, 1H), 7.30-7.10 (m, 2H), 6.86 (s, 1H), 5.98 (s, 1H), 3.834 (s, 3H), 3.62 (s, 2H), 3.19 (s, 3H), 2.33 (s, 3H), 2.29 (s, 3H), 1.25 (s, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08962834B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-9c112113a939439997b8f272871256c2 |
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| Source note | uspto-grants-2015_02 |
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