Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethylenediamine | HCID 3301 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | HCID 71286078 | HCID 71286078 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 71285814 | HCID 71285814 | 83% |
Reaction Steps
2-(6-Fluoro-1-methyl-1H-indazol-3-yl)-5-(2-trimethylsilanyl-ethoxymethyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acid [2-hydroxy-1-methyl-2-(tetrahydro-pyran-4-yl)-ethyl]-amide, diastereomer A (26 mg, 0.034 mmol) was dissolved in a 4:6 solution of TFA:DCM (5.7 mL). After stirring at room temperature overnight, the volatiles were removed under reduced pressure. The crude material was then dissolved in dichloromethane and treated with ethylenediamine (206 mg, 3.43 mmol). After stirring at room temperature overnight, water was added and the resulting precipitate was collected by filtration to afford 13 mg (83%) of 2-(6-fluoro-1-methyl-1H-indazol-3-yl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acid [2-hydroxy-1-methyl-2-(tetrahydro-pyran-4-yl)-ethyl]-amide (diastereomer A) as an off-white solid. MS: (M+H)+=453. 1H NMR (300 MHz, DMSO-d6) δ ppm 12.79 (br. s., 1H) 9.15 (s, 1H) 8.85 (dd, J=8.88, 5.48 Hz, 1H) 8.40 (s, 1H) 8.13 (d, J=9.44 Hz, 1H) 7.56-7.78 (m, 1H) 7.11-7.37 (m, 1H) 5.49 (d, J=5.67 Hz, 1H) 4.34-4.53 (m, 1H) 4.13 (s, 3H) 3.80 (d, J=10.58 Hz, 2H) 3.18-3.28 (m, 1H) 3.11 (t, J=11.14 Hz, 2H) 1.66-1.89 (m, 2H) 1.42-1.66 (m, 1H) 1.10-1.36 (m, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08658646B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-5a628264d92f448d879c2992b513785f |
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| Source note | uspto-grants-2014_02 |
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