HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 86634722, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 1-Ethylpiperazine | HCID 79196 | — |
| Reactant | HCID 24825978 | HCID 24825978 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86634722 | HCID 86634722 | 59.9% |
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), 1-ethylpiperazine (0.1164 mL, 0.9164 mmol) in THF (2 mL) were reacted to provide (4-ethylpiperazin-1-yl)(2-(2-(4-methylthiazol-2-ylamino)pyridin-4-yloxy)phenyl)methanone dihydrochloride (0.05 g, 32.64% yield). 1H NMR (DMSO) δ 8.18 (d, 1H), 7.6859 (dt, 1H), 7.54 (d, 1H), 7.42 (t, 1H), 7.29 (d, 1H), 6.59 (m, 2H), 6.56 (m, 1H), 3.35-3.63 (m, 4H), 3.12 (m, 2H), 2.50 (m, 4H, under DMSO), 2.22 (d, 3H), 1.22 (t, 2H); Mass spectrum (esi) m/z=424(100) (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08022222B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-3ea870a6b00045c6a4d0696170cc3a82 |
| Source note | uspto-grants-2011_09 |