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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1809045Generated: October 29, 2026

1,2-Dichloroethane → HCID 86761756, compound

https://huagongshe.com/reaction/1809045

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantHCID 10001879HCID 10001879—
Reactant5-amino-1,3-dihydrospiro[indene-2,3'-pyrrolo[2,3-b]pyridin]-2'(1'H)-oneHCID 59166722—
SolventDimethylformamideHCID 6228—
ProductHCID 86761756HCID 86761756—

Reaction Steps

A mixture of [5-{[(benzyloxy)carbonyl]amino}-2-(3,5-difluorophenyl)-6-oxopyrimidin-1(6H)-yl]acetic acid (91 mg, 0.22 mmol) [Veale et al. (1995) J. Med. Chem. 38, 98], 5-amino-1,3-dihydrospiro[indene-2,3′-pyrrolo[2,3-b]pyridin]-2′(1′H)-one (50 mg, 0.20 mmol) [Bell et al. WO 2006/031610], HOBT (34 mg, 0.22 mmol), and EDC (42 mg, 0.22 mmol) in DMF (2 mL) is stirred at ambient temperature for 18 h. The reaction mixture is purified directly by HPLC using a reversed phase C18 column and eluting with a gradient of H2O:CH3CN:CF3CO2H—90:10:0.1 to 5:95:0.1. The pure, product-containing fractions are combined and made basic with saturated aqueous NaHCO3. The resulting mixture is extracted with EtOAc (3×20 mL), and the combined organic extracts are washed with brine, dried over Na2SO4, filtered, and concentrated in vacuo to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362005B2
Source datasetuspto-grants-2013_01
ORD IDord-b6ece70dbb87452ca641dcfdfa5f157a
Source noteuspto-grants-2013_01