HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227450Generated: October 26, 2026
1-Hydroxybenzotriazole → HCID 21048633, compound
https://huagongshe.com/reaction/227450
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 5-Methyl-2-phenyl-4-oxazoleacetic acid | HCID 2775139 | — |
| Reactant | (S)-(4-benzylmorpholin-2-yl)methanamine | HCID 6932054 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21048633 | HCID 21048633 | 104.4% |
Reaction Steps
A mixture of (5-methyl-2-phenyl-oxazol-4-yl)-acetic acid (0.263 g), 1-hydroxylbenzotriazole (0.163 g), and N,N-diisopropylethylamine (0.211 ml) in N,N-dimethylformamide (3 ml) was treated with 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (0.232 g). The mixture was stirred for 5 min, treated with 1-[(2S)-4-benzylmorpholin-2-yl]methanamine (prepared in accordance with EP 0 995 746 A1; 0.192 g), and the solution was stirred at 22° C. for 18 h. The mixture was partitioned between dichloromethane (20 ml) and saturated aqueous sodium hydrogen carbonate (10 ml). The phases were separated in a hydrophobic frit; the organic phase was loaded onto a solid phase extraction cartridge (10 g SCX) and eluted with methanol, followed by 0.880 ammonia:methanol 10:90 to give the title compound as a colourless gum (0.394 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07560548B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-fc4e6cc5e97e44efaf8f680d41d5184b |
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| Source note | uspto-grants-2009_07 |
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