HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanethioic acid, S-(2-(((2R)-2-(acetylamino)-3-mercapto-1-oxopropyl)amino)ethyl)ester → HCID 516557, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanethioic acid, S-(2-(((2R)-2-(acetylamino)-3-mercapto-1-oxopropyl)amino)ethyl)ester | HCID 484333 | — |
| Reactant | HCID 11284496 | HCID 11284496 | — |
| Reactant | Dichloromethane methanol | HCID 21226129 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 516557 | HCID 516557 | 63% |
Reaction Steps
This compound is obtained by the S-detritylation of 12 (4.44 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: AcOEt/petroleum ether 50%). I-198 is isolated in the form of a white solid with a yield of 63%. Rf CH2Cl2/MeOH, 9.5/0.5): 0.38. M.p.=128-130° C. [α]D20=−24.7° (c 1.01, CHCl3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06979747B2 |
| Source dataset | uspto-grants-2005_12 |
| ORD ID | ord-74b57e04fc1042d18eaeada6d0afee5f |
| Source note | uspto-grants-2005_12 |