Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(4-hydrazinylphenyl)-4H-1,2,4-triazole | HCID 5162418 | — |
| Reactant | HCID 10829224 | HCID 10829224 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | Indole | HCID 798 | 116.4% |
Reaction Steps
A mixture of 4-(1,2,4-triazol-4-yl)phenylhydrazine (5.0 g, 28.6 mmol) and 5-[4-(tert-butyloxycarbonyl)piperazin-1-yl]pentanal dimethyl acetal (9.03 g, 28.6 mmol) in 4% sulphuric acid (150 ml) was heated at reflux for 48 h. The solution was cooled in an ice-bath, basified with solid K2CO3 and extracted with butan-1-ol (×3). The solvent was removed under vacuum and azeotroped with hexane (×2). The crude product was purified by chromatography on silica gel eluting with CH2Cl2 /MeOH/NH3 (30:8:1) to give the title-indole (3.9 g, 44%). δ(360 MHz, oxalate salt in D2O) 2.12-2.24 (2H, m, CH2); 2.93 (2H, t, J=7 Hz, CH2); 3.46-3.76 (8H, m, 4 of CH2) 7.37 (1H, dd, J=1.9 and 8.7 Hz, Ar-H); 7.39 (1H, s, Ar-H); 7.66 (1H, d, J=8.7, Ar-H); 7.82 (1H, d, J=1.9 Hz, Ar-H); 9.13 (2H, s, Triazole-H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05981529 |
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| Source dataset | uspto-grants-1999_11 |
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| ORD ID | ord-111e539db6354bd08e4b2dc10513d351 |
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| Source note | uspto-grants-1999_11 |
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