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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1184163Generated: November 4, 2026

Diisopropylethylamine → HCID 58355520, compound

https://huagongshe.com/reaction/1184163

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1,3-Benzothiazole-2-carboxylic acidHCID 585053—
ReactantChloro-N,N,N',N'-tetramethylformamidinium HexafluorophosphateHCID 10989639—
Reactanttert-Butyl (3S,5R)-3-(isobutylamino)-5-(morpholine-4-carbonyl)piperidine-1-carboxylateHCID 59356577—
SolventAcetonitrileHCID 6342—
SolventSodium BicarbonateHCID 516892—
ProductHCID 58355520HCID 5835552080.8%

Reaction Steps

1,3-Benzothiazole-2-carboxylic acid (29 mg), tert-butyl (3S, 5R)-3-[(2-methylpropyl)amino]-5-(morpholin-4-ylcarbonyl)piperidine-1-carboxylate (50 mg) and N,N-diisopropylethylamine (118 μl) were dissolved in acetonitrile (3 ml), chloro-N,N,N′,N′-tetramethylformamidinium hexafluorophosphate (57 mg) was added at 0° C., and the mixture was stirred at room temperature for 2 hr. The reaction mixture was diluted with 10% aqueous sodium bicarbonate, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was subjected to silica gel column chromatography, and a fraction eluted with ethyl acetate-hexane (1:1-1:0) was concentrated under reduced pressure to give the object product (58 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08664380B2
Source datasetuspto-grants-2014_03
ORD IDord-f8b6c993aab544bca3f423ec849c4680
Source noteuspto-grants-2014_03