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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1611645Generated: October 31, 2026

S-(2-Aminoethyl) ethanethioate--hydrogen chloride (1/1) → HCID 11398716, compound

https://huagongshe.com/reaction/1611645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantS-(2-Aminoethyl) ethanethioate--hydrogen chloride (1/1)HCID 519453—
ReactantHCID 7408363HCID 7408363—
ReactantHCID 22253943HCID 22253943—
ReactantS-(2-Aminoethyl) benzenecarbothioate--hydrogen chloride (1/1)HCID 45048998—
SolventEthyl ether methylene chlorideHCID 21881112—
ProductHCID 11398716HCID 1139871686%

Reaction Steps

The coupling reaction of 7 (7.4 mmol) with S-pivaloylcysteamine 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.=212-213° 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%). 11 is collected in the form of a colorless foam with a yield of 86%. Rf (AcOEt/petroleum ether, 7/3): 0.5. [α]D20=+8.5° (c 1.29, CHCl3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06989372B1
Source datasetuspto-grants-2006_01
ORD IDord-e465c681a8d34d5a95c0290db8cd52a5
Source noteuspto-grants-2006_01