Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 57590729 | HCID 57590729 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 57463080 | HCID 57463080 | 109.4% |
Reaction Steps
((R)-3-(4-{6-[3-(5-Methyl-[1,2,4]oxadiazol-3-yl)-phenyl]-imidazo[2,1-b]thiazol-5-yl}-pyrimidin-2-ylamino)-piperidine-1-carboxylic acid tert-butyl ester (0.15 g, 0.269 mmol) was dissolved in 2 mL of ethyl acetate and treated with 2 ml of 3.0 M HCl in ethyl acetate at room temperature (RT) overnight. Solid product was filtered, washed ethyl acetate and dried under vacuum overnight to provide 0.135 g (100%) of the title compound as a yellow solid. M.p.=203-207° C. 400 MHz 1H NMR (DMSO-d6 at 60° C.) δ: 9.35 (br. s, 1H), 8.21 (s, 1H), 8.12 (d, J=6.0 Hz, 1H), 8.0 (d, J=7.6 Hz, 1H), 7.82-7.80 (m, 1H), 7.67 (t, J=8.2 Hz, 1H), 7.54 (s, 1H), 6.90 (bs, 1H), 6.48 (d, J=5.6 Hz, 1H), 4.2 (br. s, 1H), 3.40 (d, J=10.8 Hz, 1H), 3.13 (d, 1H), 2.92-2.87 (m, 2H), 2.65 (s, 3H), 2.00-1.97 (m, 1H), 1.96-1.89 (m, 1H), 1.89-1.80 (bs, 1H), 1.64-1.57 (m, 1H); LCMS: 459 [M+H]. calc. for C23H22N8OS.2.3HCl: C, 50.93; H, 4.52; N, 20.66. Found C, 50.93; H, 4.42; N, 19.30.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07501430B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-a248a620d0164213b25a65efa3042531 |
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| Source note | uspto-grants-2009_03 |
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