HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814631Generated: November 2, 2026
1-Hydroxybenzotriazole → HCID 178500824, compound
https://huagongshe.com/reaction/1814631
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methyl beta-alanate | HCID 192794 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | HCID 178453065 | HCID 178453065 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178500824 | HCID 178500824 | — |
Reaction Steps
Trans-4-{[N-(tert-butoxycarbonyl)-N-(4-tert-butylcyclohexyl)amino]methyl}benzoic acid (22.0 g, 56.5 mmol) and 1-hydroxybenzotriazole (8.6 g, 57.0 mmol, containing 12% w/w water) was dissolved in DMF (300 mL). N-Dimethylaminopropyl-N′-ethylcarbodiimide hydrochloride (10.9 g, 56.8 mmol), β-alanine methyl ester (8.4 g, 60 mmol) and diisopropylethylamine (25 mL, 142 mmol) were added and the clear solution stirred at 20° C. for 16 hours. Solvent was removed by rotary evaporation and the residual oil re-dissolved in ethyl acetate (500 mL). The organic phase was washed with 5% aqueous sodium hydrogen carbonate solution (2×500 mL), 0.5 M citric acid (2×250 mL) and brine before being dried with anhydrous Na2SO4. Solvent was removed and the residual oil evaporated twice from acetonitrile. The oil was used without further purification. Yield: 24.0 g (89%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06875760B2 |
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| Source dataset | uspto-grants-2005_04 |
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| ORD ID | ord-ba167cd03f8744f8af631f0a91197d4f |
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| Source note | uspto-grants-2005_04 |
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