Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Butylamine | HCID 8007 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | N-Hydroxysuccinimide | HCID 80170 | — |
| Reactant | HCID 69529788 | HCID 69529788 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 69528746 | HCID 69528746 | — |
Reaction Steps
4 g (0.0013 mole) of (2S)-2-tert-butoxycarbonylamino-7-hydroxycarbonylmethoxy-tetralin and 1.66 g (0.0143 mole) of N-hydroxysuccinimide in 40 ml of acetonitrile were stirred at ambient temperature for 3 hours and 2.95 g (0.0143 mole) of DCC (dicyclohexylcarbodiimide) in 15 ml of ethyl ether were added. 1.3 ml (0.0195 mole) of n-butylamine were then added and it was stirred at ambient temperature overnight. The solvent was evaporated off, the residue was taken up in water; it was extracted with ethyl acetate. The organic phase was washed with an aqueous sodium bicarbonate solution, dried and the solvent was evaporated off under reduced pressure. The residue was taken up in a 1:1 ethyl acetate/hexane mixture; the precipitate formed was filtered off and oven dried. The product of the heading was obtained as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07030160B2 |
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| Source dataset | uspto-grants-2006_04 |
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| ORD ID | ord-21e56bcc7ae94d299a07ff44ec7c731b |
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| Source note | uspto-grants-2006_04 |
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