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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 46538Generated: October 30, 2026

Ammonia → HCID 178512860, compound

https://huagongshe.com/reaction/46538

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantHCID 178512859HCID 178512859—
SolventWaterHCID 962—
ProductHCID 178512860HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04173704
Source datasetuspto-grants-1979_11
ORD IDord-a55a9cf73e0b49fe981615a73913a1ce
Source noteuspto-grants-1979_11