Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | N-Hydroxysuccinimide | HCID 80170 | — |
| Reactant | N-[tert-butoxycarbonyl]-L-serine | HCID 98766 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane methanol | HCID 21226129 | — |
| Solvent | DCM MeOH AcOH | HCID 21877243 | — |
| Product | HCID 15929376 | HCID 15929376 | — |
Reaction Steps
A solution comprising 6.15 g (30 mmol) of N-Boc-L-serine (1, Fluka) and 3.45 g of N-hydroxysuccinimide (30 mmol) in 80 ml of DMF is stirred at 0° C. and 6.2 g (30 mmol) of DCC are added. The reaction mixture is maintained at 0° C. for 15 min, then it is allowed to return to ambient temperature and stirring is continued for 1 h 30. 2.75 ml (60 mmol) of ethanolamine are subsequently added. After stirring for 12 h, the DCU formed is filtered off and washed with 2×15 ml of DMF. The combined organic phases are evaporated to dryness under vacuum. The product is isolated from the residual paste by flash chromatography on a silica gel column (Kieselgel Merck 60, 230-400 mesh; eluent: CH2Cl2/MeOH 6%). The expected compound is collected in the form of a gum which crystallizes from an AcOEt/hexane mixture to provide 5.21 g (Yd=70%) of colorless needles. Rf (CH2Cl2/MeOH, 9.3/0.7): 0.23; (CH2Cl2/MeOH/AcOH, 9/0.9/0.1): 0.47. M.p.=74-76° C. [α]D20=−2.2° (c 0.9, CHCl3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06979747B2 |
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| Source dataset | uspto-grants-2005_12 |
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| ORD ID | ord-5d751103246f4f25a01771b7aa1b05ff |
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| Source note | uspto-grants-2005_12 |
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