HuagongsheHuagongshe Chemistry Print Report · For research reference only
(S)-N-Butylpyrrolidine-2-carboxamide → HCID 178449505, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (S)-N-Butylpyrrolidine-2-carboxamide | HCID 22691332 | — |
| Reactant | HCID 178514453 | HCID 178514453 | — |
| Reactant | N-cbz-l-histidyl azide | HCID 178514642 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178449505 | HCID 178449505 | — |
Reaction Steps
To 75 ml of an ethyl acetate solution of Nα -benzyloxycarbonyl-L-histidine azide (4) prepared from 4.85 g of Nα -benzyloxycarbonyl-L-histidine hydrazide (3) by the method of Reference example 2 was added 2.23 g of compound (31) under ice-cooling and the mixture was placed overnight in a refrigerator to complete the reaction. The reaction mixture was concentrated and the residue was subjected to silica gel column chromatography. By eluting the product with chloroform-methanol-aqueous ammonia (95:5:0.5), 4.13 g of Nα -benzyloxycarbonyl-L-histidyl-N-butyl-L-prolinamide was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04610821 |
| Source dataset | uspto-grants-1986_09 |
| ORD ID | ord-e9c8a3fc903b42bfbfd38a0591a1a898 |
| Source note | uspto-grants-1986_09 |