HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2172973Generated: October 27, 2026
Diisopropylethylamine → HCID 52917353, compound
https://huagongshe.com/reaction/2172973
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| Reactant | 1-(3-Bromophenyl)cyclopropanamine | HCID 11127564 | — |
| Reactant | 1-(4-Fluorophenyl)-1H-pyrazolo[3,4-c]pyridine-4-carboxylic acid | HCID 59278137 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 52917353 | HCID 52917353 | — |
Reaction Steps
To a solution of 1-(4-fluoro-phenyl)-1H-pyrazolo[3,4-c]pyridine-4-carboxylic acid (0.500 g, 1.94 mmol), 1-(3-bromophenyl)cyclopropanamine (453 mg, 2.14 mmol) and N,N-diisopropylethylamine (1.73 mL, 9.72 mmol) in DMF (18 mL) is added TBTU (0.780 g, 2.43 mmol). After 2 hours, the mixture is concentrated in vacuo, dissolved in ethyl acetate (200 mL), and washed with 2N sodium hydroxide (3×100 mL), saturated aqueous ammonium chloride (2×100 mL), saturated aqueous sodium bicarbonate (100 mL), brine (100 mL). The organic layer is dried over MgSO4, filtered through a pad of silica gel eluting with ethyl acetate (3×100 mL), and concentrated in vacuo. The residue is purified by silica gel chromatography eluting with a gradient of 50-70% ethyl acetate in heptane to give a solid that is triturated with methylene chloride to afford the title compound as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09056858B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-3ffc21f2a46e46839c2ddfc2a323d2ec |
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| Source note | uspto-grants-2015_06 |
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