HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butanol → HCID 67399111, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Dimethylamine, hydrochloride | HCID 10473 | — |
| Reactant | 2-[(4-{2-[(5-Bromopyrimidin-2-yl)(heptyl)amino]ethyl}-1,3-thiazol-2-yl)thio]-2-methylpropionic acid tert-butyl ester | HCID 59759032 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67399111 | HCID 67399111 | — |
Reaction Steps
A compound obtained using 2-[(4-{2-[(5-bromopyrimidin-2-yl)(heptyl)amino]ethyl}-1,3-thiazol-2-yl)thio]-2-methylpropionic acid tert-butyl ester synthesized in Example 442-1 and dimethylamine hydrochloride as starting materials and by an operation similar to that of Example 442-2 (solvent was changed to tert-butanol) was treated with dichloromethane and trifluoroacetic acid. The reaction solution was concentrated under reduced pressure, and the residue was purified by silica gel chromatography (elution solvent; chloroform:methanol=10:1) to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08026370B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-1d22266dad3e44acaa0715c7ae6b9cc4 |
| Source note | uspto-grants-2011_09 |