HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337233Generated: October 28, 2026
Diisopropylethylamine → HCID 71632163, compound
https://huagongshe.com/reaction/337233
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-(N-Boc-amino)piperidine | HCID 723833 | — |
| Reactant | 4-(Bromomethyl)benzenesulfonyl chloride | HCID 2734409 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 71632163 | HCID 71632163 | 70% |
Reaction Steps
Diisopropylethylamine (0.99 ml, 5.6 mmol) was added in one portion to a stirred solution of piperidin-4-yl-carbamic acid tert-butyl ester (0.37 g, 1.85 mmol) in DCM (20 ml) at room temperature. To this mixture was added 4-bromomethyl-benzenesulfonyl chloride (0.5 g, 1.85 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 (50 ml) and washed sequentially with HCl (1M solution, 20 ml), NaOH (1M solution, 20 ml) and brine (20 ml). The organic layer was separated, dried (MgSO4), filtered and concentrated. The resulting solid was collected by filtration, washed with diethyl ether and dried under vacuum to give the title compound (0.56 g, 70% yield) as an off-white solid. Tr=2.12 min, m/z (ES+) (M+Na)+ 457.
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-7c0a003d78464e2db36809a2d9d88e3c |
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| Source note | uspto-grants-2014_11 |
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