HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 178431957, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | HCID 24825978 | HCID 24825978 | — |
| Reactant | HCID 178419017 | HCID 178419017 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178431957 | HCID 178431957 | 101.3% |
Reaction Steps
Using the method of Example 32, 2-(2-(4-methylthiazol-2-ylamino)pyridin-4-yloxy)benzoic acid (0.1 g, 0.3055 mmol), triethylamine (0.2129 mL, 1.527 mmol), ethyl carbonochloridate (0.03213 mL, 0.3360 mmol), and histamine (0.1019 g, 0.9164 mmol) were reacted in THF (2 mL) to provide N-(2-(1H-imidazol-4-yl)ethyl)-2-(2-(4-methylthiazol-2-ylamino)pyridin-4-yloxy)benzamide dihydrochloride (0.084 g, 55.17% yield). 1H NMR (CDCl3) δ 8.38 (s, 1H), 8.08 (d, 1H), 7.76 (d, 1H), 7.51 (t, 1H), 7.39 (t, 1H), 7.06 (s, 1H), 7.02 (m, 2H), 6.89 (s, 1H), 6.55 (m, 2H), 3.81 (m, 2H), 3.16 (m, 2H), 2.45 (s, 3H); Mass spectrum (esi) m/z=421 (100) (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08022222B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-7a25526c07274fe8b80d2292763d4d83 |
| Source note | uspto-grants-2011_09 |