HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → HCID 178523867, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | (S)-N-(2-Hydroxyethyl)pyrrolidine-2-carboxamide | HCID 12136434 | — |
| Reactant | HCID 178514453 | HCID 178514453 | — |
| Reactant | N-cbz-l-histidyl azide | HCID 178514642 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178523867 | HCID 178523867 | — |
Reaction Steps
To an ethyl acetate solution of Nα -benzyloxycarbonyl-L-histidinazide (4) prepared from Nα -benzyloxycarbonyl-L-histidine hydrazide (3) (6.07 g) by a known method was added 10 ml of a DMF solution of 2.31 g of (S)-N-(2-hydroxyethyl)-2-pyrrolidinecarboxamide (53) under ice-cooling and they were reacted overnight in a refrigerator. The reaction mixture was concentrated and the residue thus formed was subjected to silica gel column chromatography. By eluting the product with chloroform-methanol-aqueous ammonia (90:10:1), 3.43 g of Nα -benzyloxycarbonyl-L-histidyl-N-(2-hydroxyethyl)-L-prolinamide (54) was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04610821 |
| Source dataset | uspto-grants-1986_09 |
| ORD ID | ord-fd0484b57bd14994b07788ba22b8ef20 |
| Source note | uspto-grants-1986_09 |