HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1013015Generated: November 1, 2026
1,2-Dichloroethane → HCID 54684202, compound
https://huagongshe.com/reaction/1013015
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | HCID 67316527 | HCID 67316527 | — |
| Catalyst | Diacetyloxymercury | HCID 16683746 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Propargylamine | HCID 239041 | — |
| Product | HCID 54684202 | HCID 54684202 | — |
Reaction Steps
To a solution of lithium (3-(benzyloxy)-2-{[(4-fluorobenzyl)amino]carbonyl}-9,9-dimethyl-4-oxo-4,6,7,9-tetrahydro-8H-pyrazino[1,2-a]pyrimidin-8-yl)acetate (1 eq.) in CHCl3, propargylamine (1.1), EDC (2 eq.) and HOBt (2 eq.) were added and the reaction mixture was stirred at room temperature for 3 hours. The solvent was removed under reduced pressure and the residue was taken up in EtOAc, washed with brine, dried (Na2SO4), and concentrated under reduced pressure. The resulting crude was directly dissolved in acetic acid and Hg(OAc)2 (0.1 eq.) was added. The mixture was heated at 100° C. overnight and was then concentrated under reduced pressure. The residue was directly purified by RP-HPLC and after lyophilisation of the desired fractions, the O-benzyl protected material was dissolved in MeOH and stirred 1 hour under an H2 atmosphere in the presence of 10% Pd/C. The catalyst was then filtered off through celite, the filtrate was concentrated under reduced pressure and then the residue was dissolved in MeCN and H2O and lyophilized to afford the titled oxazole. 1H-NMR (400 MHz, d6-DMSO) δ 12.17 (br. s, 1H), 9.43 (t, J=6.2 Hz, 1H), 7.37 (dd, J=8.1 Hz, J=5.7 Hz, 2H), 7.17 (t, J=8.9 Hz, 2H), 6.77 (s, 1H), 4.47 (d, J=6.2 Hz, 2H), 3.80 (s, 2H), 3.71 (t, J=5.0 Hz, 2H), 3.00 (t, J=5.1 Hz, 2H), 2.27 (s, 3H), 1.53 (s, 6H); MS (ES) C22H24FN5O4 requires 441. Found: 442 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07981879B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-68d79960d52d492f8f969ba917092b08 |
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| Source note | uspto-grants-2011_07 |
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