HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1519161Generated: November 3, 2026
4-(Bromomethyl)phenylacetic acid → HCID 77844320, compound
https://huagongshe.com/reaction/1519161
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-(Bromomethyl)phenylacetic acid | HCID 4519056 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 90310688 | HCID 90310688 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 77844320 | HCID 77844320 | 10.5% |
Reaction Steps
A solution of 6-cyclobutyl-3-(3,4-dihydro-2H-pyrido[3,2-b][1,4]oxazin-7-yl)-2-fluorophenol (50 mg, 0.17 mmol) and 2-(4-(bromomethyl)phenyl)acetic acid (38 mg, 0.17 mmol) in DMSO (1 mL) was treated with potassium tert-butoxide (38 mg, 0.33 mmol) and stirred for 16 hours at 80° Celsius. The reaction was then cooled to rt, filtered, and the filtrate subjected directly to HPLC purification to give (4-{[6-cyclobutyl-3-(3,4-dihydro-2H-pyrido[3,2-b][1,4]oxazin-7-yl)-2-fluorophenoxy]methyl}phenyl)acetic acid (8 mg, 9%). MS (ESI): mass calcd. for C26H25FN2O4, 448.18; m/z found, 449.2 [M+H]+. 1H NMR (600 MHz, CD3OD) δ 7.72 (s, 1H), 7.60 (s, 1H), 7.40 (d, J=8.1, 2H), 7.31 (d, J=8.1, 2H), 7.19 (d, J=6.0, 2H), 5.04 (s, 2H), 4.38-4.32 (m, 2H), 3.78-3.72 (m, 1H), 3.71-3.67 (m, 2H), 3.63 (s, 2H), 2.29-2.22 (m, 2H), 2.16-2.07 (m, 2H), 2.04-1.97 (m, 1H), 1.84 (t, J=9.6, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09073876B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-3ce1549ca06d4f58b4354470a7ce1915 |
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| Source note | uspto-grants-2015_07 |
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