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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1611644Generated: November 1, 2026

S-(2-Aminoethyl) ethanethioate--hydrogen chloride (1/1) → HCID 516560, compound

https://huagongshe.com/reaction/1611644

Reaction equation

Participants

RoleNameHCIDCharge
ReactantS-(2-Aminoethyl) ethanethioate--hydrogen chloride (1/1)HCID 519453—
Reactant(2R)-2-acetamido-3-((triphenylmethyl)sulfanyl)propanoic acidHCID 7408363—
ReactantEthyl ether methylene chlorideHCID 21881112—
ReactantHCID 22253953HCID 22253953—
ReactantS-(2-Aminoethyl) benzenecarbothioate--hydrogen chloride (1/1)HCID 45048998—
ProductHCID 516560HCID 51656080%

Reaction Steps

The coupling reaction of 7 (4.5 mmol) with S-isobutyrylcysteamine hydrochloride [(compound obtained according to the same methods as those described by T. Wieland and E. Bokelman, Ann. Chem., 1952, 576; 20-34; during the syntheses of S-acetylcysteamine hydrochloride and S-benzoylcysteamine hydrochloride) M.p.=147-148° C.] is carried out according to method B described in the first synthetic route (example 1). After the various treatments, the expected compound is isolated by flash chromatography on a silica gel column (eluent: CH2Cl2/ether 30%). 10 is collected in the form of a colorless foam with a yield of 80%. Rf (AcOEt/petroleum ether, 8/2): 0.37. [α]D20=+10° (c 1.1, CHCl3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06989372B1
Source datasetuspto-grants-2006_01
ORD IDord-52085b210826408e9e71a539277db754
Source noteuspto-grants-2006_01