HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1631733Generated: November 3, 2026
1-Hydroxybenzotriazole → HCID 86670119, compound
https://huagongshe.com/reaction/1631733
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 1-Phenethylamine, (-)- | HCID 75818 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | HCID 86670107 | HCID 86670107 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 86670119 | HCID 86670119 | — |
Reaction Steps
To a 50 mL round-bottom flask were added 4-(5-bromo-2-chloropyrimidin-4-yl)morpholine-3-carboxylic acid (PREPARATION x30, 300 mg, 0.930 mmol), 1-hydroxybenzotriazole (126 mg, 0.930 mmol), and (S)-1-phenylethanamine (118 μl, 0.930 mmol) in 1,4-dioxane (9.3 mL) to give a green solution. 1-Ethyl-(3-dimethylaminopropyl)carbodiimide hydrochloride (178 mg, 0.930 mmol) was added to the solution, which was allowed to react at room temperature for 6 hours. The mixture was subsequently partitioned between aqueous saturated NaHCO3 and ethyl acetate. The aqueous layer was extracted with ethyl acetate and the combined organic layers were dried over MgSO4, filtered, and concentrated to give the title compound, which was used without further purification. ESI-MS m/z [M+H]+ calc'd for C17H18BrClN4O2, 425.03. found 425.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08791107B2 |
|---|
| Source dataset | uspto-grants-2014_07 |
|---|
| ORD ID | ord-99846c8c3aee4e259a5c74b7f642d2a7 |
|---|
| Source note | uspto-grants-2014_07 |
|---|