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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 710166Generated: October 25, 2026

N-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)picolinamide → Isopropyl 4-{5-[6-(methylcarbamoyl)pyridin-3-yl]benzo[d]oxazol-2-yl}piperidine-1-carboxylate

https://huagongshe.com/reaction/710166

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)picolinamideHCID 44119560—
ReactantIsopropyl 4-(5-bromobenzo[d]oxazol-2-yl)piperidine-1-carboxylateHCID 71257568—
ProductIsopropyl 4-{5-[6-(methylcarbamoyl)pyridin-3-yl]benzo[d]oxazol-2-yl}piperidine-1-carboxylateHCID 712572605.8%

Reaction Steps

Following the General Procedure-1, the titled compound (20 mg) was prepared from Intermediate 13 (300 mg, 0.82 mmol) and N-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)picolinamide (256 mg, 0.98 mmol) as a brown solid. M.P.: 158-161° C. MS (m/z): 423.5 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181214B2
Source datasetuspto-grants-2015_11
ORD IDord-ac475505ca714dffa884cb922dd6c260
Source noteuspto-grants-2015_11