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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2196175Generated: October 29, 2026

Methylamine → HCID 24877276, compound

https://huagongshe.com/reaction/2196175

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantTetrahydrofuranHCID 8028—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
ReactantHCID 24877383HCID 24877383—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 24877276HCID 24877276—

Reaction Steps

To a stirred solution of 2-{[(3E)-3-(5,5-dimethyl-4-morpholin-4-ylfuran-2(5H)-ylidene)-2-oxo-2,3-dihydro-1H-indol-6-yl]thio}benzoic acid in 5 mL of anhydrous DMF, were added 2M methylamine in THF solution (0.066 mL, 0.13 mmol), HBTU (49 mg, 0.13 mmol) and DIPEA (31 mg, 0.24 mmol). The reaction mixture was stirred at room temperature for 15 minutes and poured into 100 mL of water. The precipitates were filtered, washed with water and dried to give the crude product as a brown solid. Purification of the crude product by silica gel chromatography eluted with a gradient of 5-15% MeOH in CHCl3 afforded 2-{[(3E)-3-(5,5-dimethyl-4-morpholin-4-ylfuran-2(5H)-ylidene)-2-oxo-2,3-dihydro-1H-indol-6-yl]thio}-N-methylbenzamide as brown solid. Yield: 6 mg, 12%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338415B2
Source datasetuspto-grants-2012_12
ORD IDord-4e9993ef2adf4588a27fa0e8972b595d
Source noteuspto-grants-2012_12