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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1990880Generated: October 30, 2026

Ethyl 4-amino-1-piperidinecarboxylate → HCID 68699686, compound

https://huagongshe.com/reaction/1990880

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-amino-1-piperidinecarboxylateHCID 100867—
ReactantMethyl 2-chloro-1,3-benzoxazole-7-carboxylateHCID 68406054—
SolventAcetonitrileHCID 6342—
ProductHCID 68699686HCID 6869968695.5%

Reaction Steps

To a solution of 2-chloro-benzooxazole-7-carboxylic acid methyl ester (0.43 g, 2.05 mmol, 1.0 equiv) in acetonitrile (30 mL) was added ethyl 4-amino-1-piperidine carboxylate (0.64 g, 3.08 mmol, 1.5 equiv) and the reaction mixture heated to reflux for 30 min. The solvent was removed under reduced pressure and the crude material purified with column chromatography on silica eluting with dichloromethane/methanol (4:1) to afforded 0.68 g (95%) of the title compound. 1H NMR (300 MHz, DMSO): δ 1.19 (t, J=7.0 Hz, 3H), 1.38-1.51 (m, 2H), 1.95-2.00 (m, 2H), 2.96-3.03 (m, 2H), 3.78-3.81 (m, 1H), 3.89 (s, 3H), 3.82-3.96 (m, 2H), 4.04 (q, J=7.0 Hz, 2H), 7.23 (t, J=7.9 Hz, 1H), 7.50 (dd, J=7.9 Hz, J=1.9 Hz, 2H), 8.34 (d, J=7.3 Hz, 2H). 13C NMR (75 MHz, DMSO): δ 14.54, 31.01, 42.04, 49.71, 52.05, 60.63, 112.36, 119.98, 121.27, 123.51, 144.77, 147.00, 154.57, 162.13, 164.17. MS (ISP): 347.9 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07645753B2
Source datasetuspto-grants-2010_01
ORD IDord-f076ad4bcd7d4c9bb8562b790a2ff017
Source noteuspto-grants-2010_01