HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 178496437, compound → HCID 178496438, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 178496437 | HCID 178496437 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | HCID 178496438 | HCID 178496438 | 65.9% |
Reaction Steps
(RS)-[1-Amino-1-[4-({2-methoxy-2-[l -(2-trimethylsilanyl-ethoxymethyl)-1H-benzoimidazol-2-yl]-acetylamino }-methyl)-phenyl]-meth-(E)-ylidene]-carbamic acid benzyl ester (0.5 g) was heated in 5 N HCl (20 ml) to 50° C. and stirring at that temperature was continued for 4 h. After cooling to r.t., the mixture was washed with EtOAc and cooled to 0° C. The pH was brought to ˜12 by the dropwise addition of 4 N NaOH. The mixture was then extracted with EtOAc. The combined organics were washed with brine, dried (MgSO4), filtered and concentrated to give (RS)-[1-amino-1-(4-{[2-(1H-benzoimidazol-2-yl)-2-methoxy-acetylamino]-methyl}-phenyl)-meth-(E)-ylidene]-carbamic acid benzyl ester (0.258 g) as light yellow solid. MS472.3 ([M+H]+)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07056932B2 |
| Source dataset | uspto-grants-2006_06 |
| ORD ID | ord-55aae54022074ee7903c8cd28ec35b3e |
| Source note | uspto-grants-2006_06 |