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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1486711Generated: November 1, 2026

Water → HCID 131736801, compound

https://huagongshe.com/reaction/1486711

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CarbonateHCID 10340—
ReactantMethylboronic AcidHCID 139377—
ReactantHCID 131736802HCID 131736802—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 131736801HCID 131736801—

Reaction Conditions

Temperature100 °C

Reaction Steps

Methylboronic acid (23.2 mg, 0.377 mmol) and a solution of 2 M Na2CO3 (0.088 mL, 0.502 mmol) is added to a solution of 1-(3-bromo-5-nitro-benzyl)-piperidine-4-carboxylic acid tert-butylamide BB-10a (100 mg, 0.251 mmol) in anhydrous toluene (3 mL) The mixture is purged under argon for 15 min. Tetrakis(triphenylphosphine)palladium (0) (58 mg, 0.0502 mmol) is added and the mixture is heated to 100° C. overnight. Water (10 mL) and AcOEt (10 mL) are added and the aqueous phase is extracted twice with AcOEt (10 mL). The combined organic phases are dried over MgSO4, filtered and concentrated under reduced pressure. The title compound is obtained by prep. LC-MS F as a colorless powder (61 mg, 73%); LC-MS A: tR=0.63 min; [M+H]+=334.24.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09428456B2
Source datasetuspto-grants-2016_08
ORD IDord-03c2a160ff9c4d33be6a5a2a4a53f3ed
Source noteuspto-grants-2016_08