HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1918503Generated: October 31, 2026
4-(4-Chloro-2-fluorobenzyloxy)pyridin-2(1H)-one → HCID 66603505, compound
https://huagongshe.com/reaction/1918503
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-(4-Chloro-2-fluorobenzyloxy)pyridin-2(1H)-one | HCID 58092257 | — |
| Reactant | HCID 58092313 | HCID 58092313 | — |
| Product | HCID 66603505 | HCID 66603505 | 53.7% |
Reaction Steps
2-Bromo-11-methyl-5,7,8,9,9a,10-hexahydro-11H-pyrido[3′,2′:4,5]pyrrolo[3,2-f]indolizine (150 mg, 0.491 mmol) and 4-(4-chloro-2-fluorobenzyloxy)pyridin-2(1H)-one (124 mg, 0.491 mmol) were reacted following the procedure for Example 2 (step b) to provide the title compound (68 mg, 27%) as a yellow solid: mp 210-220° C.; 1H NMR (500 MHz, DMSO-d6) δ 10.95 (s, 1H), 8.06 (d, J=8.3 Hz, 1H), 7.84-7.82 (d, J=7.8 Hz, 1H), 7.65-7.62 (t, J=Hz, 1H), 7.56-7.53 (dd, J=9.9, 2.0 Hz, 1H), 7.39-7.37 (m, 2H), 6.17-6.16 (dd, J=7.8, 2.7 Hz, 1H), 6.06 (d, J=2.7 Hz, 1H), 5.20 (s, 2H), 4.82-4.78 (dd, J=14.0, 2.4 Hz, 1H), 4.35-4.30 (m, 1H), 3.91-3.71 (m, 5H), 3.50 (m, 1H), 3.30-3.26 (m, 1H), 3.12-3.06 (m, 1H), 2.47-2.42 (m, 1H), 2.19-2.07 (m, 2H), 1.93-1.86 (m, 1H); ESI MS m/z 479 [M+H]+; HPLC (Method B) 98.1% (AUC), tR=13.9 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08618299B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-755233b474534456b347ef5aeb419c0d |
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| Source note | uspto-grants-2013_12 |
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