HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 66615864, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Pivaloyl chloride | HCID 62493 | — |
| Reactant | Methyl 2-((1r,4r)-4-(4-(5-aminopyridin-2-yl)phenyl)cyclohexyl)acetate | HCID 66615773 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 66615864 | HCID 66615864 | — |
Reaction Steps
To a mixture of {4-[4-(5-amino-pyridin-2-yl)-phenyl]-cyclohexyl}-acetic acid methyl ester (100 mg, 0.3 mmol) in methylene chloride (10 ml) was added triethylamine (43 ul, 0.3 mmol) and trimethylacetyl chloride (40 ul, 0.3 mmol). After 15 hours at room temperature, the reaction was diluted with hexanes to afford a precipitate which was collected by filtration: 1H NMR (400 MHz, DMSO-d6) δ ppm 1.15 (dd, J=12.69, 1.71 Hz, 2 H) 1.26 (s, 10 H) 1.42-1.56 (m, 1 H)1.50 (d, J=9.85 Hz, 1 H) 1.82 (d, J=11.37 Hz, 5 H) 2.26 (d, J=6.69 Hz, 2 H) 3.61 (s, 3 H) 7.32 (d, J=8.34 Hz, 2H) 7.87 (d, J=8.72 Hz, 1 H) 7.95 (d, J=8.34 Hz, 2 H) 8.15 (dd, J=8.72, 2.53 Hz, 1 H) 8.88 (d, J=2.53 Hz, 1 H)9.53 (s, 1 H); (M+H)+ 409.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08912208B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-b426c8f649334e45858d7b8e68bf4f04 |
| Source note | uspto-grants-2014_12 |