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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337207Generated: October 29, 2026

Diisopropylethylamine → HCID 71079542, compound

https://huagongshe.com/reaction/337207

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4-(N-Boc-amino)piperidineHCID 723833—
Reactant1-CYCLOPROPANECARBONYL-2,3-DIHYDRO-1H-INDOLE-5-SULFONYL CHLORIDEHCID 20109462—
SolventDichloromethaneHCID 6344—
ProductHCID 71079542HCID 7107954280.1%

Reaction Steps

Diisopropylethylamine (0.33 ml, 2.0 mmol) was added in one portion to a stirred solution of piperidin-4-yl-carbamic acid tert-butyl ester (0.2 g, 1.0 mmol) in DCM (5 ml) at room temperature. To this mixture was added 1-cyclopropanecarbonyl-2,3-dihydro-1H-indole-5-sulfonyl chloride (0.29 g, 1.0 mmol) in one portion and the mixture was stirred at room temperature under a nitrogen atmosphere for 1 hour. After this time the mixture was diluted with DCM (100 ml) and washed sequentially with HCl (1M solution, 50 ml), NaOH (1M solution, 50 ml) and brine (50 ml). The organic layer was separated, dried (MgSO4), filtered and concentrated. The resulting solid was collected by filtration, dried with diethyl ether and dried under vacuum give the title compound (0.36 g, 73% yield) as a pale yellow solid. Tr=2.02 min m/z (ES+) (M+Na+) 472.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889716B2
Source datasetuspto-grants-2014_11
ORD IDord-3803567d6395441ea1072359d014d073
Source noteuspto-grants-2014_11