Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 57820116 | HCID 57820116 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 50942502 | HCID 50942502 | 24% |
Reaction Steps
(E)-[2-(3-{4-[[Formyl-(2-morpholin-4-yl-ethyl)-amino]-(4-trifluoromethyl-phenylcarbamoyl)-methyl]-phenyl}-acryloylamino)-phenyl]-carbamic acid tert-butyl ester (300 mg, 0.432 mmol) was treated with 1.25M HCl in methanol (2.6 mL) at room temperature overnight. The reaction was quenched slowly with solid sodium bicarbonate until the pH was 6-7. The mixture was diluted in acetonitrile with a small amount of dimethylsulfoxide, passed through a 40 μm pipette filter, and then purified by preparative HPLC to obtain the desired product (58 mg, 24%). MS: calc'd 568 (MH+) exp 568 (MH+). 1H NMR (d6-DMSO, 400 MHz) δ 10.6 (broad s, 1H), 9.40 (s, 1H), 7.84 (d, 2H, J=8.4 Hz), 7.69 (d, 2H, J=8.4 Hz), 7.62 (d, 2H, J=8.0 Hz), 7.54 (d, 2H, J=8.0 Hz), 7.53 (d, 1H, J=15.6 Hz), 7.33 (d, 1H, J=7.6 Hz), 6.91 (t, 1H, J=7.6 Hz), 6.89 (d, 1H, J=15.6 Hz), 6.75 (d, 1H, J=7.2 Hz), 6.58 (t, 1H, J=7.2 Hz), 4.94 (broad s, 2H), 4.51 (broad s, 1H), 3.59 (m, 4H), 3.45 (m, 2H), 2.66 (m, 2H), 2.33 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07795315B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-88badcfc0b2e408698f77540d07f514e |
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| Source note | uspto-grants-2010_09 |
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