HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 889223Generated: November 2, 2026
HCID 66760610, compound → HCID 66759342, compound
https://huagongshe.com/reaction/889223
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 66760610 | HCID 66760610 | — |
| Reactant | HCID 66761194 | HCID 66761194 | — |
| Product | HCID 66759342 | HCID 66759342 | 53% |
Reaction Steps
4-((2-fluorobenzyl)oxy)-2-methylquinolin-8-ol from step 1 was reacted with 5-(3-((2-((2,4-dichloro-3-(chloromethyl)phenyl)(methyl)amino)-2-oxoethyl)amino)-3-oxopropyl)-N-methylpicolinamide as described previously to give 5-(3-((2-((2,4-dichloro-3-(((4-((2-fluorobenzyl)oxy)-2-methylquinolin-8-yl)oxy)methyl)phenyl)(methyl)amino)-2-oxoethyl)amino)-3-oxopropyl)-N-methylpicolinamide in 53% yield. MS (+APCI) 718 (M+). 1H-NMR (CDCl3, δ ppm): 8.36 (s, 1H), 8.07 (d, J=8.0 Hz, 1H), 7.95 (bd, 1H), 7.94 (d, J=8.0 Hz, 1H), 7.63 (m, 1H), 7.58 (m, 1H), 7.45 (d, J=8.4 Hz, 1H), 7.36 (t, J=8.0 Hz, 1H), 7.25 (m, 4H), 7.15 (m, 1H), 7.05 (m, 1H), 6.77 (bs, 1H), 6.40 (bt, 1H), 5.62 (s, 2H), 5.38 (s, 2H), 3.76 (dd, J=5.2, 17.6 Hz, 1H), 3.46 (dd, J=3.6, 18 Hz, 1H), 3.22 (s, 3H), 3.00 (m, 6H), 2.69 (m, 2H), 2.56 (t, 2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08252793B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-e26c1bc4b2564c209a79e1bd185c71d1 |
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| Source note | uspto-grants-2012_08 |
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