Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | HCID 57033312 | HCID 57033312 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86601682 | HCID 86601682 | — |
Reaction Steps
2 g (5.26 mmol) of (3S)-3-{[(benzyloxy)carbonyl]amino}-6-[(tert-butoxycarbonyl) amino]hexanoic acid and 0.56 g (5.73 mmol) of triethylamine are dissolved in 30 ml of THF under argon and cooled to 0° C. 0.59 g (5.73 mmol) of ethyl chloroformate are added, and the mixture is stirred at 0° C. for 3 hours. The reaction mixture is filtered through kieselguhr, and the filtrate is reacted directly.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07655643B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-be48c5c4a0c6491682844ca5beaea8e6 |
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| Source note | uspto-grants-2010_02 |
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