HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → HCID 178523866, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | (S)-N-[3-(2-oxo-1-pyrrolidinyl)propyl]-2-pyrrolidinecarboxamide | HCID 53958674 | — |
| Reactant | HCID 178514453 | HCID 178514453 | — |
| Reactant | N-cbz-l-histidyl azide | HCID 178514642 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178523866 | HCID 178523866 | — |
Reaction Steps
To 30 ml of a ethyl acetate solution of compound (4) prepared from 2.12 g of compound (3) by a known method was added 5 ml of a DMF solution of 1.17 g of compound (100) under ice-cooling and the reaction was maintained 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), 2.00 g of Nα -benzyloxycarbonyl-L-histidyl-N-[3-(2-oxo-1-pyrrolidinyl)-propyl]-L-prolinamide (101) was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04564609 |
| Source dataset | uspto-grants-1986_01 |
| ORD ID | ord-9c73004689364a89b023e62f72125263 |
| Source note | uspto-grants-1986_01 |