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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 71029Generated: October 28, 2026

Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) → (S)-2-(3,5-dimethylphenylacetamido)-3-phenyl-N-[4-(7-(2-morpholin-4-yl-ethoxy)-imidazo[2,1-b]benzothiazol-2-yl)phenyl]propanamide

https://huagongshe.com/reaction/71029

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant2-(4-Aminophenyl)-7-(2-morpholin-4-yl-ethoxy)imidazo[2,1-b]-[1,3]benzothiazoleHCID 44598669—
ReactantHCID 67042063HCID 67042063—
SolventDimethylformamideHCID 6228—
Product(S)-2-(3,5-dimethylphenylacetamido)-3-phenyl-N-[4-(7-(2-morpholin-4-yl-ethoxy)-imidazo[2,1-b]benzothiazol-2-yl)phenyl]propanamideHCID 51038974—

Reaction Conditions

Temperature155 °C

Reaction Steps

Working as in the example 4, but using (S)-2-(2-(3,5-dimethylphenyl)acetamido)-3-phenyl-propionic acid and [4-(7-(2-morpholin-4-yl-ethoxy)imidazo[2,1-b]benzothiazol-2-yl]aniline and reagents as HATU and DIPHEA in dry DMF. The reaction mixture was stirred at room temperature for 6 h, at 70° C. for 48 h and at 155° C. for 24 h. Then the solvent was removed under reduced pressure and the crude mixture was purified by flash chromatography to give the desired product (S)-2-(3,5-dimethylphenylacetamido)-3-phenyl-N-[4-(7-(2-morpholin-4-yl-ethoxy)-imidazo[2,1-b]benzothiazol-2-yl)phenyl]propanamide

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822698B2
Source datasetuspto-grants-2014_09
ORD IDord-f157c2c822394b9d8657eb2f9a53d913
Source noteuspto-grants-2014_09