HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1690693Generated: October 31, 2026
3-Chloro-2-fluoroaniline → HCID 16046966, compound
https://huagongshe.com/reaction/1690693
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Chloro-2-fluoroaniline | HCID 75014 | — |
| Reactant | (4-Fluoro-3-methylphenyl)boronic acid | HCID 2774580 | — |
| Reactant | HCID 57618475 | HCID 57618475 | — |
| Reactant | HCID 66904603 | HCID 66904603 | — |
| Product | HCID 16046966 | HCID 16046966 | — |
Reaction Steps
The title material is prepared by reacting N-[3-(5-Oxo-5,6,7,8-tetrahydro-naphthalen-2-yl)-phenyl]-methanesulfonamide and (4′-Fluoro-3′-methyl-biphenyl-3-yl)-hydrazine hydrochloride (prepared as in example 70, steps 1 and 2 except using 3-methyl-4-fluorophenylboronic acid and 3-chloro-2-fluoroaniline as the coupling partners) in an analogous manner to example 1, step 3 except that purification is accomplished by reverse phase UV triggered HPLC: 1H NMR (400 MHz, d6-DMSO) δ 12.66 (s, 1H), 9.88 (s, 1H), 8.82 (d, J=8.7 Hz, 1H), 8.31 (m, 1H), 8.29 (d, J=8.6 Hz, 1H), 8.08 (d, J=8.2 Hz, 1H), 7.94 (m, 1H), 7.80 (d, J=8.6 Hz, 1H), 7.66 (m, 1H), 7.61 (m, 2H), 7.48 (m, 1H), 7.30 (m, 2H), 3.09 (m, 2H), 3.04 (s, 3H), 2.97 (m, 2H), 2.08 (s, 3H); LC/MS calculated for [M+H]+ C30H25F2N2O2S: 515.6, found: 515.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08153671B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-acbd724494394699923b4372090468aa |
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| Source note | uspto-grants-2012_04 |
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