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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2098378Generated: November 1, 2026

Pyridine → N-(3-(1H-tetrazol-5-yl)phenyl)-4-methyl-1-(5-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)piperidine-4-carboxamide

https://huagongshe.com/reaction/2098378

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantOxalyl chlorideHCID 65578—
Reactant1-[(Tert-butoxy)carbonyl]-4-methylpiperidine-4-carboxylic acidHCID 23282848—
Reactanttert-butyl 4-(3-(1H-tetrazol-5-yl)phenylcarbamoyl)-4-methylpiperidine-1-carboxylateHCID 178451883—
ReactantHCID 178507542HCID 178507542—
CatalystDimethylformamideHCID 6228—
Solvent1,1-DichloroethaneHCID 6365—
ProductN-(3-(1H-tetrazol-5-yl)phenyl)-4-methyl-1-(5-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)piperidine-4-carboxamideHCID 17843082170%

Reaction Steps

Preparation of tert-butyl 4-(3-(1H-tetrazol-5-yl) phenylcarbamoyl)-4-methylpiperidine-1-carboxylate. To a solution of 1-(tert-butoxycarbonyl)-4-methylpiperidine-4-carboxylic acid (100 mg, 0.41 mmol) in dichloroethane (2.0 mL) were added DMF (2 drops) and pyridine (0.13 g, 1.6 mmol), followed by oxalyl chloride (57 mg, 0.45 mmol). The mixture was stirred for 40 minutes, and 3-(1H-tetrazol-5-yl)-phenylamine was added. The mixture was stirred for 2 hours, and a pink precipitate formed. The mixture was filtered, and the filtrate was washed with 1.0 N aq. HCl and brine, dried over MgSO4, and concentrated to give the title compound in 70% yield. MS (ES+) [M+H]+=387.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450332B2
Source datasetuspto-grants-2013_05
ORD IDord-9d162513bbcd4a0683d0ad05d111630f
Source noteuspto-grants-2013_05