HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1273046Generated: October 27, 2026
3-Amino-1-propanol → [3-(4-Fluorophenyl)(1h-indazol-5-yl)]-n-(3-hydroxypropyl)carboxamide
https://huagongshe.com/reaction/1273046
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Amino-1-propanol | HCID 9086 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| Reactant | 3-(4-Fluorophenyl)-1H-Indazole-5-Carboxylic Acid | HCID 22260722 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [3-(4-Fluorophenyl)(1h-indazol-5-yl)]-n-(3-hydroxypropyl)carboxamide | HCID 20789056 | 78.5% |
Reaction Steps
The title compound was prepared as described in Example 76. To a solution of 3-(4-fluorophenyl)-1H-indazole-5-carboxylic acid (0.200 g, 0.781 mmol) in tetrahydrofuran (5 mL) was added 1-hydroxybenzotriazole hydrate (0.316 g, 2.34 mmol) followed by 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (0.449 g, 2.34 mmol), 3-amino-1-propanol (0.178 mL, 2.34 mmol) and N,N-dimethylformamide (2 mL). The solution was stirred for 16 h at room temperature. Water (40 mL) was added and the solid was filtered and dried in a vacuum oven to give the title compound (0.192 g, 78% yield): 1H NMR (DMSO-d6) δ 13.45 (s, 1H), 8.59 (t, 1H), 8.53 (s, 1H), 8.08 (AB quartet, 2H), 7.91 (dd, 1H), 7.62 (d, 1H), 7.40 (t, 2H), 4.50 (t, 1H), 3.48 (q, 2H), 3.36 (q, 2H), 1.71 (pentet, 2H); ES-MS (m/z) 314 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07208513B2 |
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| Source dataset | uspto-grants-2007_04 |
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| ORD ID | ord-6636dc6191bd4f98b5c6cd4a5dd263ca |
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| Source note | uspto-grants-2007_04 |
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