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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1888514Generated: November 3, 2026

2-Methoxyethanol → HCID 58266777, compound

https://huagongshe.com/reaction/1888514

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethoxyethanolHCID 8019—
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant8-(Benzenesulfonyl)-12-bromo-3-hydroxy-5,8,10-triazatricyclo[7.4.0.02,7]trideca-1(9),2,4,6,10,12-hexaene-4-carbonitrileHCID 58266472—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 58266777HCID 5826677737%

Reaction Steps

A solution of 9-benzenesulfonyl-3-bromo-5-hydroxy-9H-dipyrido[2,3-b;4′,3′-d]pyrrole-6-carbonitrile (120 mg, 0.28 mmol), 2-methoxyethanol (128 μL, 1.60 mmol) and triphenylphosphine (315 mg, 1.60 mmol) in anhydrous DMF (1.25 mL) was treated dropwise with diethyl azodicarboxylate (252 μL, 1.60 mmol) and the mixture stirred at ambient temperature for 9 h. The mixture was diluted with ethyl acetate (15 mL) and washed with brine (3×10 mL), dried over anhydrous magnesium sulfate, filtered and evaporated in vacuo. The crude material was purified by column chromatography (silica, 5 g column, Si-SPE, 30-50% DCM in pentane) to afford the title compound (50 mg, 37%). 1H NMR (CDCl3, 400 MHz): 9.58 (s, 1H), 8.97 (d, J=2.3 Hz, 1H), 8.76 (d, J=2.3 Hz, 1H), 8.24-8.22 (m, 1H), 8.22-8.00 (m, 1H), 7.66-7.60 (m, 1H), 7.54-7.48 (m, 2H), 4.74-4.69 (m, 2H), 3.87-3.83 (m, 2H), 3.48 (s, 3H). LCMS (Method B): RT=4.25 min, M+H+=487/489.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501765B2
Source datasetuspto-grants-2013_08
ORD IDord-9f5ca0ffbe13436fa9c60cc277e539f6
Source noteuspto-grants-2013_08