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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1640293Generated: October 29, 2026

Diisopropylethylamine → 5-(6-(2,3-dihydro-1H-pyrrolo[2,3-b]pyridin-1-carbonyl)pyrimidin-4-ylamino)-1,3-dihydro-spiro[indene-2,3'-pyrrolo[2,3-b]pyridin]-2'(1'H)-one

https://huagongshe.com/reaction/1640293

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant1H,2H,3H-pyrrolo(2,3-b)pyridineHCID 10011889—
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—
SolventDimethylformamideHCID 6228—
Product5-(6-(2,3-dihydro-1H-pyrrolo[2,3-b]pyridin-1-carbonyl)pyrimidin-4-ylamino)-1,3-dihydro-spiro[indene-2,3'-pyrrolo[2,3-b]pyridin]-2'(1'H)-oneHCID 49801672—

Reaction Steps

150 mg (0.37 mmol) 6-(2′-oxo-1,1′,2′,3-tetrahydrospiro[indene-2,3′-pyrrolo[2,3-b]pyridin]-5-ylamino)pyrimidine-4-carboxylic acid hydrochloride, 50 mg (0.42 mmol) 2,3-dihydro-1H-pyrrolo[2,3-b]pyridine, 0.15 mL (0.87 mmol) DIPEA and 130 mg (0.41 mmol) TBTU in 1.8 mL DMF were stirred overnight at RT. The purification was carried out by preparative HPLC-MS. The product-containing fractions were combined and lyophilised. Then the substance was dissolved in DMF and purified again by preparative HPLC-MS. The product-containing fractions were combined and lyophilised.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08110575B2
Source datasetuspto-grants-2012_02
ORD IDord-8aad0523b0f243fc8b65e50278e4bec1
Source noteuspto-grants-2012_02