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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 873609Generated: October 30, 2026

1-[(Benzyloxy)carbonyl]azetidine-3-carboxylic acid → HCID 86702125, compound

https://huagongshe.com/reaction/873609

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-[(Benzyloxy)carbonyl]azetidine-3-carboxylic acidHCID 10988214—
Reactanttert-Butyl 4-(4-aminophenoxy)piperidine-1-carboxylateHCID 22181157—
ReactantHCID 86702126HCID 86702126—
ProductHCID 86702125HCID 86702125—

Reaction Steps

The title compound was prepared as described in Example 1A, substituting aniline for tert-butyl 4-(4-aminophenoxy)piperidine-1-carboxylate and 4-(1-(pyridazin-3-yl)azetidine-3-carboxamido)benzoic acid for 1-(benzyloxycarbonyl)azetidine-3-carboxylic acid. 1 H NMR (400 MHz, DMSO-d6/D2O) δ ppm 8.53 (dd, J=4.4, 1.3 Hz, 1H), 7.98-7.92 (m, 2H), 7.77-7.65 (m, 5 H), 7.38-7.24 (m, 3 H), 7.15-7.07 (m, 1H), 4.49 (t, J=9.0 Hz, 2H), 4.46-4.38 (m, 2H), 4.00-3.81 (m, 1H); MS (ESI(+)) m/e 374 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975398B2
Source datasetuspto-grants-2015_03
ORD IDord-4a8865e12178469580fee8dc7945ce88
Source noteuspto-grants-2015_03