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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1640271Generated: October 26, 2026

Dimethylformamide → N-(dicyclopropylmethyl)-N-methyl-6-(2'-oxo-1,1',2',3-tetrahydrospiro[indene-2,3'-pyrrolo-[2,3-b]pyridin]-5-ylamino)pyrimidine-4-carboxamide

https://huagongshe.com/reaction/1640271

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantDiisopropylethylamineHCID 81531—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant6-(2'-Oxo-1,1',2',3-tetrahydrospiro[indene-2,3'-pyrrolo[2,3-b]pyridin]-5-yl-amino)pyrimidine-4-carboxylic acid-hydrochlorideHCID 66722185—
ProductN-(dicyclopropylmethyl)-N-methyl-6-(2'-oxo-1,1',2',3-tetrahydrospiro[indene-2,3'-pyrrolo-[2,3-b]pyridin]-5-ylamino)pyrimidine-4-carboxamideHCID 49800516—

Reaction Steps

1.2 equivalents (12 μmol) of the amine derivative, 3.4 equivalents DIPEA (34 μmol) and 1.20 equivalents (12 μmol) TBTU were added to 4.1 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 RT. The reaction mixture was evaporated down at 60° C. in a vacuum centrifuge. The following compounds were able to be synthesised analogously to this working method:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08110575B2
Source datasetuspto-grants-2012_02
ORD IDord-a70baaeca1f0483bb37a3d186ede802d
Source noteuspto-grants-2012_02