HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 491968Generated: October 29, 2026
1-Hydroxybenzotriazole → HCID 57462011, compound
https://huagongshe.com/reaction/491968
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1H-Imidazole-2-carboxylic acid | HCID 574321 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | tert-Butyl alaninate hydrochloride | HCID 11275390 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 57462011 | HCID 57462011 | 73% |
Reaction Steps
To a solution of 1H-imidazole-2-carboxylic acid (0.179) in N,N-dimethylformamide (DMF) (3 mL) was added alanine tert-butyl ester hydrochloride (0.22 g), diisopropylethyl amine (0.27 mL) and HOBT (0.41 g) before cooling to 0° C. and the reaction mixture was then treated with EDC HCl (0.32 g). The cooling bath was removed and the reaction mixture was stirred at ambient temperature for 18 hrs before being diluted with ethyl acetate and washed with water and brine, dried (MgSO4) and concentrated at reduced pressure. The residue was purified by silica gel chromatography (30% ethyl acetate in hexanes) to afford the sub-title compound as a colourless oil (0.263 g, 73%): 1H NMR 400 MHz CDCl3 1.50 (9H, s), 1.51 (3H, d, J 7.2), 3.70 (1H, m), 7.28 (2H, s), 7.78 (1H, d, J 7.6), 11.49 (1H, br s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07531570B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-e53f7512f786428ba6b874eaf11eccad |
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| Source note | uspto-grants-2009_05 |
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