HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylamine → HCID 86693471, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | 1-Ethynylcyclopentanol | HCID 87074 | — |
| Reactant | HCID 86693469 | HCID 86693469 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86693471 | HCID 86693471 | — |
| Product | HCID 86693472 | HCID 86693472 | — |
Reaction Steps
9-fluoro-3-(hydroxy(1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazol-5-yl)methyl)-104(1-hydroxycyclopentyl)ethynyl)-6,7-dihydro-5H-5,7-methanobenzo[c]imidazo[1,2-a]azepine-2-carboxamide was prepared similarly according to General Procedure E with slight modification. 10-bromo-9-fluoro-3-(hydroxy(1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazol-5-yl)methyl)-6,7-dihydro-5H-5,7-methanobenzo[c]imidazo[1,2-a]azepine-2-carboxamide was reacted with 1-ethynylcyclopentanol in a solution of DMF (1.3 mL/mmol) and diisopropylamine (2.6 mL/mmol) to afford the title compound which was carried forward to the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09034866B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-a32b3df9c97946e2a302f29924e43eef |
| Source note | uspto-grants-2015_05 |