HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → HCID 178512860, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | HCID 178512859 | HCID 178512859 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178512860 | HCID 178512860 | — |
Reaction Steps
Nα -(3-benzoylthiopropanoyl)-L-arginine (1 g.) is dissolved with vigorous stirring in a mixture of water (5 ml.) and concentrated ammonia (5 ml.). After one hour, the solution is extracted with ethyl acetate and concentrated to dryness in vacuo. The residue is chromatographed on a column of DEAE Sephadex [anion exchange resin derived from dextran (Mikes, supra, page 328)] (85 ml.) with a buffer of 0.005 M ammonium bicarbonate. The fractions containing the Nα -(3-mercaptopropanoyl)-L-arginine (as indicated by positive thiol and Sakaguchi Reaction) are pooled and lyophilized to remove ammonium bicarbonate, yield 200 mg., m.p. 230° (starts decomposing at 200°).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04173704 |
| Source dataset | uspto-grants-1979_11 |
| ORD ID | ord-a55a9cf73e0b49fe981615a73913a1ce |
| Source note | uspto-grants-1979_11 |