HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dabco → HCID 59655715, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dabco | HCID 9237 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-tert-Butyl-3-hydroxyazetidine | HCID 287986 | — |
| Reactant | HCID 59655729 | HCID 59655729 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59655715 | HCID 59655715 | — |
Reaction Steps
To a solution of 1-tert-butylazetidin-3-ol (19 mg, 0.15 mmol), 1,4-diazabicyclo[2.2.2]octane (11 mg, 0.10 mmol), and diisopropylethylamine (0.026 ml, 0.15 mmol) in tetrahydrofuran (1 ml) was added 4-chloro-7-(2-chlorophenyl)-8-(4-chlorophenyl)-2-methylpyrazolo[1,5-a][1,3,5]triazine (I-2A-1b; 39 mg, 0.10 mmol), portionwise. After stirring for 2 days, the reaction was concentrated, in vacuo, and the residue purified on a Biotage™ Flash 12S column using 20-40% ethyl acetate in hexanes to afford 11A-1 (25 mg, 52%) as a solid: +APcI MS (M+1) 482.3; 1H NMR (400 MHz, CD3OD) δ 7.52-7.42 (m, 4H), 7.39 (d, J=8.3 Hz, 2H), 7.24 (d, J=8.3 Hz, 2H), 5.58 (quintet, J=6.2 Hz, 1H), 3.80-3.75 (m, 2H), 3.63-3.58 (m, 2H), 2.60 (s, 3H), 1.04 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07329658B2 |
| Source dataset | uspto-grants-2008_02 |
| ORD ID | ord-2f0f535158c64fe5830d189d275ecda4 |
| Source note | uspto-grants-2008_02 |