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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1394928Generated: November 2, 2026

Triethylamine → HCID 86605054, compound

https://huagongshe.com/reaction/1394928

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Amino-1-Boc-piperidineHCID 1268291—
ReactantHCID 59682327HCID 59682327—
SolventDichloromethaneHCID 6344—
ProductHCID 86605054HCID 86605054—

Reaction Steps

Crude 18-2 (115 mg, 0.24 mmol) was suspended in anhydrous CH2CL2 (3 mL) and treated successively with 4-amino-1-tert-butyloxycarbonyl-piperidine (235 mg, 1.17 mmol) and Et3N (0.1 mL, 0.7 mmol). The suspension was stirred for 6 hours and complete dissolution was observed. Upon completion, the reaction was diluted further with CH2Cl2 (20 mL) and washed with 1N HCl to remove all unbound amine and Et3N. The organic layer was dried (MgSO4), filtered and concentrated under reduced pressure to yield crude 18-3 as a yellow oil: LRMS m/z (N C(CH3)3+H) 427.9 found, 428.1 required.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07348440B2
Source datasetuspto-grants-2008_03
ORD IDord-9d670c402433424d85712068ca9111ae
Source noteuspto-grants-2008_03