HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372244Generated: October 30, 2026
Hydrazine hydrate (1:1) → HCID 21069852, compound
https://huagongshe.com/reaction/1372244
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | HCID 21069796 | HCID 21069796 | — |
| Reactant | HCID 21069851 | HCID 21069851 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21069852 | HCID 21069852 | 54% |
Reaction Steps
A stirred solution of intermediate 65, 2-[3-(3-trifluoromethyl-diaziridin-3-yl)-benzyl]-isoindole-1,3-dione, (150 mg, 0.43 mmol) in ethanol (2 mL) was treated with hydrazine hydrate (0.4 mL) at room temperature and the solution stirred for 3.5 hrs. After removing ethanol in vacuo, the residue was partitioned between CH2Cl2 and water. The aqueous phase was acidified with dilute HCl, and washed with CH2Cl2. The aqueous phase was basified with dilute NaOH, and extracted with CH2Cl2. The organic extract was dried (MgSO4), filtered, and concentrated to obtain 50 mg (Yield 54%) of (3-(3-(trifluoromethyl)diaziridin-3-yl)phenyl)methanamine and (3-(3-(trifluoromethyl)-3H-diazirin-3-yl)phenyl)methanamine as a 1:1 mixture; 1H NMR (300 MHz, CDCl3) δ ppm: 3.85 (2H, s) 3.88 (2H, s) 7.08 (2H, s) 7.31–7.40 (4H, m) 7.43–7.50 (1H, m, J=6.2 Hz) 7.54 (1H, s); LC/MS m/z 216 (M+H for diazirine) and 218 (M+H for diaziridine).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07157447B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-007cad3dcc364269824bf58fa29f22c5 |
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| Source note | uspto-grants-2007_01 |
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