HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1640298Generated: November 2, 2026
Diisopropylethylamine → HCID 49801981, compound
https://huagongshe.com/reaction/1640298
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| 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 | 6-(2'-Oxo-1,1',2',3-tetrahydrospiro[indene-2,3'-pyrrolo[2,3-b]pyridin]-5-yl-amino)pyrimidine-4-carboxylic acid-hydrochloride | HCID 66722185 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 49801981 | HCID 49801981 | — |
Reaction Steps
1.2 equivalents (12 μmol) of the amine derivative, 3.4 equivalents DIPEA (34 μmol) and 1.2 equivalents (12 μmol) HATU were added to 4.10 mg (10 μmol) 6-(2′-oxo-1,1′,2′,3-tetrahydrospiro[indene-2,3′-pyrrolo[2,3-b]pyridin]-5-ylamino)pyrimidine-4-carboxylic acid hydrochloride in 0.32 mL DMF and the mixture was shaken overnight at 80° C. The reaction mixture was evaporated down in the vacuum centrifuge at 60° C. The following compounds were able to be synthesised analogously to this working method:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08110575B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-43443ad50038466eaddfd5c06ce54825 |
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| Source note | uspto-grants-2012_02 |
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