HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 750297Generated: November 3, 2026
N-(3-Aminopropyl)morpholine → HCID 69155751, compound
https://huagongshe.com/reaction/750297
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-(3-Aminopropyl)morpholine | HCID 61055 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | HCID 69157027 | HCID 69157027 | — |
| Reactant | HCID 178526939 | HCID 178526939 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 69155751 | HCID 69155751 | — |
Reaction Steps
To a solution (2 ml) of 4-(4-carboxyphenyl)-6-chloro-2-(4-methanesulfonylbenzyl)-1-oxo-1,2-dihydroisoquinoline-3-carboxylic acid methyl ester (100 mg) and 3-morpholin-4-ylpropylamine (31 μl) in acetonitrile were added 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (69 mg) and 4-hydroxybenzotriazole monohydrate (38 mg) at room temperature with stirring, and the mixture was stirred at room temperature for 12 hrs. The solvent was removed under reduced pressure, and the residue was partitioned between ethyl acetate and 1N hydrochloric acid. The organic layer was dried and concentrated to dryness. The residue was purified by silica gel column chromatography (ethyl acetate/methanol=10/1) to give the title compound (93 mg) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07402595B2 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-e276d2960dd240f49136f7646818a091 |
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| Source note | uspto-grants-2008_07 |
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