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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1505442Generated: November 2, 2026

Dimethylformamide → HCID 67966832, compound

https://huagongshe.com/reaction/1505442

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant(2R)-2-[(2-methylpropan-2-yl)oxycarbonylamino]butanoic acidHCID 2755936—
Reactant6-(Spiro[1-benzofuran-3,1'-cyclopropan]-4-yloxy)-3-pyridinamineHCID 67235459—
ProductHCID 67966832HCID 6796683289.5%

Reaction Steps

To a solution of (2R)-2-({[(1,1-dimethylethyl)oxy]carbonyl}amino)butanoic acid (94 mg, 0.462 mmol) in dry N,N-Dimethylformamide (2 mL) DIPEA (0.115 mL, 0.661 mmol) and then TBTU (159 mg, 0.496 mmol) were added and the reaction mixture was stirred for 15 minutes at room temperature. 6-(spiro[1-benzofuran-3,1′-cyclopropan]-4-yloxy)-3-pyridinamine (Reference Intermediate 216, 84 mg) was added and the reaction mixture was stirred for 6 hours at the same temperature. The reaction was quenched with brine (2 ml), diluted with water (5 ml) and extracted with ethyl acetate (2×10 ml). The organic layer was washed with ice cold brine (2×5 ml), dried over sodium sulphate, filtered and evaporated. The residue was purified by flash chromatography (Biotage system) on silica gel using a 10 g SNAP column and cyclohexane to cyclohexane/ethyl acetate 7:3 as eluents affording the title compound as a colourless oil (130 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216967B2
Source datasetuspto-grants-2015_12
ORD IDord-a36df87903664decabac65ebe82680ac
Source noteuspto-grants-2015_12