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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 969807Generated: October 26, 2026

2-Phenylbenzoxazole-4-carboxylic acid → N-(1-Methylpiperidin-4-yl)-2-phenylbenzoxazole-4-carboxamide

https://huagongshe.com/reaction/969807

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Phenylbenzoxazole-4-carboxylic acidHCID 10868369—
Reactant1-Methylpiperidin-4-amine dihydrochlorideHCID 22002536—
ProductN-(1-Methylpiperidin-4-yl)-2-phenylbenzoxazole-4-carboxamideHCID 1163138838%

Reaction Steps

N-(1-Methylpiperidin-4-yl)-2-phenylbenzoxazole-4-carboxamide was prepared from 2-phenylbenzoxazole-4-carboxylic acid and 4-amino-1-methylpiperidine dihydrochloride using the conditions described for Step C in Example 1. This compound was obtained in 38% yield as a white solid; mp 126-128° C.; 1H NMR (300 MHz, CDCl3) δ 9.26 (d, J=7.5 Hz, 1H), 8.25 (m, 2H), 8.19 (d, J=7.7 Hz, 1H), 7.70 (d, J=8.1 Hz, 1H), 7.63-7.53 (m, 3H), 7.46 (t, J=8.0 Hz, 1H), 4.20 (m, 1H), 2.86 (m, 2H), 2.37 (s, 3H), 2.33-2.13 (m, 4H), 1.85-1.73 (m, 2H); MS (APCI) m/z 336 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07307094B2
Source datasetuspto-grants-2007_12
ORD IDord-d5290a6a412746dc831adda994fab58c
Source noteuspto-grants-2007_12