HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 45704Generated: October 29, 2026
Hydrazine hydrate (1:1) → (E)-3-(3,5-difluoro-4-phenoxyphenyl)-2-methylprop-2-en-1-amine
https://huagongshe.com/reaction/45704
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | (E)-2-(3-(3,5-difluoro-4-phenoxyphenyl)-2-methylallyl)isoindoline-1,3-dione | HCID 67458948 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (E)-3-(3,5-difluoro-4-phenoxyphenyl)-2-methylprop-2-en-1-amine | HCID 67454559 | 71.9% |
Reaction Steps
To a solution of (E)-2-(3-(3,5-difluoro-4-phenoxyphenyl)-2-methylallyl)isoindoline-1,3-dione (Intermediate 93.2, 100 mg, 0.25 mmol) in methanol (1 mL) was added hydrazine hydrate (25 mg, 0.5 mmol) and the reaction stirred at 50° C. overnight. The white solid was filtered with DCM, and the solvent removed from the filtrate. The residue was brought up in DCM and filtered. This was repeated until no further precipitate formed to give 49.5 mg of the title compound (71%) as a yellow oil, a 10 mg portion of which was diluted with 1N HCl and freeze dried to give 7.8 mg of the title compound as an HCl salt. 1H-NMR (400 MHz, d6-DMSO): δ 8.25 (s, 2H), 7.37 (t, 2H), 7.20 (d, 2H), 7.12 (t, 1H), 6.97 (s, 1H), 3.57 (s, 2H), 1.96 (s, 3H). MS (m/z): 258.96 (M-NH2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08541448B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-38bc9383725b420d86e774f4b30c7983 |
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| Source note | uspto-grants-2013_09 |
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