Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Propylamine | HCID 7852 | — |
| Reactant | HCID 54193464 | HCID 54193464 | — |
| Product | Ammonium Hydroxide | HCID 14923 | — |
| Product | HCID 54230793 | HCID 54230793 | 179.8% |
Reaction Steps
To a solution of (S)-N-{2-[5-[2-(7-aza-bicyclo[2.2.1]hept-7-yl)-1,1-dimethyl-2-oxo-ethyl]-2-(3,5-dimethylphenyl)-1H-indol-3-yl]-propyl}-N-(2-morpholin-4-yl-ethyl)-2,4-dinitrobenzenesulfonamide (61.3 mg in 1.4 mL dry methylene chloride) was added 0.130 mL of n-propylamine and the mixture stirred at room temperature. After 60 minutes the reaction was quenched by the addition of water, extracted with ethyl acetate and the combined organics washed with saturated aqueous sodium bicarbonate. The organic portion was then dried over sodium sulfate and concentrated in vacuo. Purification of the residue by flash chromatography on silica gel (methylene chloride:methanol, 92:8; then methylene chloride:methanol:ammonium hydroxide, 90:7:1) gave the title compound (39 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06017944 |
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| Source dataset | uspto-grants-2000_01 |
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| ORD ID | ord-279f9d8cd01f40ab821a4095cd165f10 |
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| Source note | uspto-grants-2000_01 |
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