HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanethioic acid, S-(2-(((2R)-2-(acetylamino)-3-mercapto-1-oxopropyl)amino)ethyl)ester → HCID 86593958, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanethioic acid, S-(2-(((2R)-2-(acetylamino)-3-mercapto-1-oxopropyl)amino)ethyl)ester | HCID 484333 | — |
| Reactant | Ethyl ether methylene chloride | HCID 21881112 | — |
| Reactant | HCID 87919653 | HCID 87919653 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 86593958 | HCID 86593958 | 70% |
Reaction Steps
This compound is obtained by the S-detritylation of 14 (2.56 mmol). The protocol used is the same as that described in example 1 for the synthesis of I-152. After the various treatments, a gum is collected, which gum is purified by flash chromatography on a silica gel column (eluent: CH2Cl2/ether 30%). I-203 is isolated in the form of white solid with a yield of 70%. Rf CH2Cl2/ether, 5/5): 0.44. M.p.=117-120° C. [α]D20=−36.5° (c 1.04, CHCl3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06979747B2 |
| Source dataset | uspto-grants-2005_12 |
| ORD ID | ord-15bc0e6f6b9a4cd9be218d26a67cfe5c |
| Source note | uspto-grants-2005_12 |