HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1867010Generated: October 31, 2026
HCID 22050178, compound → HCID 22050179, compound
https://huagongshe.com/reaction/1867010
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 22050178 | HCID 22050178 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 22050179 | HCID 22050179 | 64% |
Reaction Steps
A solution of 3-Bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-({5-[(4-methylpiperazin-1-yl)carbonyl]pyrazin-2-yl}methyl)pyridin-2(1H)-one trifluoroacetate (0.17 g, 0.00026 mol) in 0.1N NaOH (25 mL) was stirred at room temperature for 15 min. and extracted the product in ethyl acetate (2×20 mL). The combined organic extracts were washed with water (2×20 mL), dried (Na2SO4) and concentrated to dryness. The residue was dried in vacuo to afford the title product (0.09 g, 64%) as a white powder: 1H NMR (CD3OD/400 MHz) δ8.69 (d. 1H, J=1.2 Hz), 8.67 (d, 1H, J=1.2 Hz), 7.60 (m, 1H), 7.00 (m, 2H), 6.54 (s, 1H), 5.50 (s, 2H), 5.30 (s, 2H), 3.78 (t, 2H, J=4.8 Hz), 3.58 (t, 2H, J=4.8 Hz), 2.526 (s, 3H), 2.53 (t, 2H, J=4.8 Hz), 2.44 (t, 2H, J=4.8 Hz), and 2.31 (s, 3H); 19F NMR (CD3OD/400 MHz)=δ −111.65 (m) and −116.06 (m); ES-HRMS m/z 548.1123 (M+H C24H25N5O3BrF2 requires 548.1103).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07629363B2 |
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| Source dataset | uspto-grants-2009_12 |
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| ORD ID | ord-e6cd51cc363e4b6fa4c4177bb16954eb |
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| Source note | uspto-grants-2009_12 |
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