HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239682Generated: October 30, 2026
4-(2-Aminoethyl)benzonitrile → HCID 11682966, compound
https://huagongshe.com/reaction/2239682
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-(2-Aminoethyl)benzonitrile | HCID 21912525 | — |
| Reactant | 2-tert-Butyl-4-chloro-5-phenylisothiazol-3(2H)-one 1,1-dioxide | HCID 67242627 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 11682966 | HCID 11682966 | 16.4% |
Reaction Steps
2-tert-Butyl-4-chloro-5-phenylisothiazol-3(2H)-one 1,1-dioxide (0.175 g, 0.58 mmol), 4-(2-aminoethyl)benzonitrile (0.101 g, 0.69 mmol) and TEA (0.23 g, 2.31 mmol) was dissolved in dry DMF (3 ml) and heated in a microwave reactor at 130° C. for 30 mins. The reaction mixture was purified by preparative HPLC to yield the title compound (0.039 g, 16%). 1H NMR (500 MHz, CDCl3): δ 7.53-7.43 (m, 7H), 6.88-6.84 (m, 2H), 5.39-5.33 (m, 1H), 3.17-3.10 (m, 2H), 2.65-2.60 (m, 2H), 1.71 (s, 9H); 13C NMR (125 MHz, CDCl3): δ 159.7, 143.2, 134.7, 132.7, 131.8, 130.1, 129.5, 129.1, 125.2, 118.8, 111.1, 108.1, 61.9, 44.5, 41.2, 36.2, 27.8; Mass Spectrum: M−H+ 410.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07723333B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-553fa739da7c4366be2920efc7bfa1f2 |
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| Source note | uspto-grants-2010_05 |
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