HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2237628Generated: October 30, 2026
Dimethylformamide → HCID 178511071, compound
https://huagongshe.com/reaction/2237628
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 178513913 | HCID 178513913 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178511071 | HCID 178511071 | — |
Reaction Steps
To a stirred slurry of 2-{trans-4-[4-(4-amino-5-oxo-7,8-dihydropyrimido[5,4-f][1,4]oxazepin-6(5H)-yl)phenyl]cyclohexyl}acetamide (45 mg, 0.11 mmol), from Example 30, in THF (1 mL) was added DMF (0.002 mL) and oxalyl chloride (0.05 mL, 0.6 mmol). After two hours of stirring at room temperature, the reaction was quenched with aqueous sodium bicarbonate and extracted with EtOAc. The organic layer was washed with water, dried over sodium sulfate and concentrated in vacuo to afford the title compound as a light-yellow colored solid, 34 mg. 1H NMR (400 MHz, DMSO-d6): δ 8.17 (s, 1H), 7.63 (br s, 2H) 7.22 (m, 4H), 4.57 (m, 2H), 3.90 (m, 2H), 2.43 (m, 3H), 1.78 (m, 4H), 1.63 (m, 1H), 1.43 (m, 2H), 1.08 (m, 2H). m/z=378.3 (M+1). IC50 64.3 nM (range 51.2-91.1 nM).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07718645B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-71f421057a93497bac5947527665fa69 |
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| Source note | uspto-grants-2010_05 |
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