HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylcarbodiimide → 15-(benzyloxycarbonyl)pentadecyl 5-(Cbz-amino)-4-oxopentanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylcarbodiimide | HCID 12734 | — |
| Reactant | 4-Pyrrolidinopyridine | HCID 75567 | — |
| Reactant | 5-(((Benzyloxy)carbonyl)amino)-4-oxopentanoic acid | HCID 11369104 | — |
| Reactant | Benzyl 16-hydroxyhexadecanoate | HCID 90034516 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 15-(benzyloxycarbonyl)pentadecyl 5-(Cbz-amino)-4-oxopentanoate | HCID 90034486 | 29.2% |
Reaction Steps
This compound was prepared from the product of 15a (1.2 g; 3.2 mmol), 5-(Cbz-amino)-4-oxopentanoic acid (0.84 g; 3.2 mmol), 4-pyrrolidinylpyridine (50 mg), and N,N′-diisopropylcarbodiimide (0.50 g; 4.0 mmol) in dichloromethane (35 mL) according to Procedure D. The reaction time was 3 days. The crude product was purified on a 85×55 mm silica gel 60 column eluted with ethyl acetate-hexane (1:1) (1000 mL) collecting 13×50 mL fractions. Fractions containing the product (3-6) were evaporated and 0.57 g (29%) product was obtained (white solid, mp 78-81° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09249086B2 |
| Source dataset | uspto-grants-2016_02 |
| ORD ID | ord-9f42bb99b1f8488ea8b67cbcb295054f |
| Source note | uspto-grants-2016_02 |