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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2383060Generated: October 29, 2026

Isobutyric Acid → HCID 67538280, compound

https://huagongshe.com/reaction/2383060

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutyric AcidHCID 6590—
ReactantTriethylamineHCID 8471—
ReactantMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
ReactantHCID 67536297HCID 67536297—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 67538280HCID 67538280—

Reaction Steps

Tert-butyl 7-(aminomethyl)-1-cyclohexyl-3,4-dihydroisoquinoline-2(1H)-carboxylate (999 mg) was dissolved in methylene chloride. Isobutyric acid (0.33 mL), triethylamine (1.2 mL), and O-(benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (1.32 g) were added thereto, followed by stirring at room temperature for 18 hours. Water was added to the mixture which was then extracted with chloroform. The extract was washed with a 1 M aqueous NaOH solution and saturated brine, and dried over magnesium sulfate. The solvent was evaporated and the resulting residue was purified by silica gel column chromatography to obtain tert-butyl-1-cyclohexyl-7-[(isobutylamino)methyl]-3,4-dihydroisoquinoline-2(1H)-carboxylate (468 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263607B2
Source datasetuspto-grants-2012_09
ORD IDord-2783a2258a4048e88a14c1a8ab5d8ff5
Source noteuspto-grants-2012_09