HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25276Generated: October 29, 2026
Triethylamine → 5-isopropyl-1-methyl-1H-indazole-4-carboxylic acid indan-2-yl-(4-methyl-benzyl)-amide
https://huagongshe.com/reaction/25276
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 15637824 | HCID 15637824 | — |
| Reactant | 5-Isopropyl-1-methyl-1H-indazole-4-carbonyl chloride | HCID 22566940 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-isopropyl-1-methyl-1H-indazole-4-carboxylic acid indan-2-yl-(4-methyl-benzyl)-amide | HCID 20760448 | — |
Reaction Steps
5-Isopropyl-1-methyl-1H-indazole-4-carbonyl chloride (0.618 mmol, 1.0 eq) (30) in 5 ml of THF is added to a solution of (4-tolyl)-indan-2-yl-amine (147 mg, 0.618 mmol) (31) in 5 ml of tetrahydrofuran containing 250 mg of triethylamine at 0° C. The resulting mixture is stirred at room temperature overnight, diluted with 20 ml of ethyl acetate, washed with water and brine, and dried over sodium sulfate. Concentration and purification by silica gel chromatography affords 168 mg of 5-isopropyl-1-methyl-1H-indazole-4-carboxylic acid indan-2-yl-(4-methyl-benzyl)-amide (32). 1H NMR (400 MHz, CDCl3) 7.89 (1H, s), 7.42˜6.92 (10H, m), 4.95 (1H, d, J=15.2 Hz), 4.66 (1H, d, J=15.2 Hz), 4.551 (1H, m), 4.05 (3H, s), 3.26˜2.73 (5H, m), 2.36 (3H, s), 1.34 (6H, dd, J=1.6, 6.8Hz). MS (+VE) m/z 438 (M++1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06858637B2 |
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| Source dataset | uspto-grants-2005_02 |
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| ORD ID | ord-1c2e53d2e6464627981d6eff1862f342 |
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| Source note | uspto-grants-2005_02 |
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