Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methyl Isocyanate | HCID 12228 | — |
| Reactant | HCID 86759195 | HCID 86759195 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 56611972 | HCID 56611972 | 81% |
Reaction Steps
To a mixture of (S)-3-{[7-(3-amino-propoxy)-4-oxo-4H-quinolizine-2-carbonyl]-amino}-2-benzenesulfonylamino-propionic acid tert-butyl ester (10.0 mg, 0.015 mmol) in anhydrous acetonitrile (0.5 ml) were added triethylamine (4 μl, 0.030 mmol) and methyl isocyanate (1 μl, 0.015 mmol). The mixture was stirred for 5 minutes at 0° C. and 30 minutes at room temperature, quenched with water and extracted with dichloromethane (3x). The combined organic layers were dried (MgSC4) and concentrated to give 4.1 mg (81% yield) of desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06630488B1 |
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| Source dataset | uspto-grants-2003_10 |
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| ORD ID | ord-d5473c60c3aa47d29362475df5b90356 |
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| Source note | uspto-grants-2003_10 |
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