HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337207Generated: October 29, 2026
Diisopropylethylamine → HCID 71079542, compound
https://huagongshe.com/reaction/337207
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-(N-Boc-amino)piperidine | HCID 723833 | — |
| Reactant | 1-CYCLOPROPANECARBONYL-2,3-DIHYDRO-1H-INDOLE-5-SULFONYL CHLORIDE | HCID 20109462 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 71079542 | HCID 71079542 | 80.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08889716B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-3803567d6395441ea1072359d014d073 |
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| Source note | uspto-grants-2014_11 |
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