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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1040557Generated: October 31, 2026

Diisopropylethylamine → HCID 67391447, compound

https://huagongshe.com/reaction/1040557

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantHOAtHCID 181649—
Reactant3,3-Difluoroazetidine hydrochlorideHCID 2758247—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 67390583HCID 67390583—
SolventDimethylacetamideHCID 31374—
ProductHCID 67391447HCID 6739144745.3%

Reaction Steps

A solution of the resulting intermediate (S)-2-{[(R)-5-(4-cyano-benzyl)-7-(3,5-dichloro-phenyl)-5-methyl-6-oxo-6,7-dihydro-5H-imidazo[1,2-a]imidazole-3-carbonyl]-amino}-succinamic acid (0.039 g, 0.070 mmol) in DMA (0.5 mL) was added to a solution of 3,3-difluoroazetidine hydrochloride (0.014 g, 0.135 mmol) in DMA (0.5 mL). A solution of HOAt (0.015 g, 0.110 mmol) in DMA (0.5 mL) was added to the reaction mixture, followed by HATU (0.04 g, 0.105 mmol) in 0.5 mL DMA. The reaction mixture was agitated on an orbital shaker for 3 h. Diisopropylethylamine (0.036 mL, 0.207 mmol) was added and the resulting solution was agitated on an orbital shaker for 14 h. The volatiles were removed in vacuo at 40° C. and the crude product was dissolved in DMSO (1 mL) and water (0.1 mL) and purified via reverse phase HPLC to afford 0.020 g (45%) of (R)-5-(4-cyano-benzyl)-7-(3,5-dichloro-phenyl)-5-methyl-6-oxo-6,7-dihydro-5H-imidazo[1,2-a]imidazole-3-carboxylic acid [(S)-1-carbamoylmethyl-2-(3,3-difluoro-azetidin-1-yl)-2-oxo-ethyl]-amide as a white solid, m/z 632.3 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08552205B2
Source datasetuspto-grants-2013_10
ORD IDord-300c1dcd6f574b49868cf29322e135b5
Source noteuspto-grants-2013_10