HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1040557Generated: October 31, 2026
Diisopropylethylamine → HCID 67391447, compound
https://huagongshe.com/reaction/1040557
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HOAt | HCID 181649 | — |
| Reactant | 3,3-Difluoroazetidine hydrochloride | HCID 2758247 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | HCID 67390583 | HCID 67390583 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 67391447 | HCID 67391447 | 45.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08552205B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-300c1dcd6f574b49868cf29322e135b5 |
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| Source note | uspto-grants-2013_10 |
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