HuagongsheHuagongshe Chemistry Print Report · For research reference only
S-(2-Aminoethyl) ethanethioate--hydrogen chloride (1/1) → HCID 516560, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | S-(2-Aminoethyl) ethanethioate--hydrogen chloride (1/1) | HCID 519453 | — |
| Reactant | (2R)-2-acetamido-3-((triphenylmethyl)sulfanyl)propanoic acid | HCID 7408363 | — |
| Reactant | Ethyl ether methylene chloride | HCID 21881112 | — |
| Reactant | HCID 22253953 | HCID 22253953 | — |
| Reactant | S-(2-Aminoethyl) benzenecarbothioate--hydrogen chloride (1/1) | HCID 45048998 | — |
| Product | HCID 516560 | HCID 516560 | 80% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06989372B1 |
| Source dataset | uspto-grants-2006_01 |
| ORD ID | ord-52085b210826408e9e71a539277db754 |
| Source note | uspto-grants-2006_01 |