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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2373384Generated: October 30, 2026

4-(N-Boc-amino)piperidine → HCID 59851708, compound

https://huagongshe.com/reaction/2373384

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(N-Boc-amino)piperidineHCID 723833—
ReactantHCID 59852114HCID 59852114—
ReactantHCID 66934663HCID 66934663—
ProductHCID 59851708HCID 59851708—

Reaction Steps

In a manner similar to that described for Method N, 2-(3,4-dimethoxy-phenylamino)-6-oxo-6,7-dihydro-5H-benzo[b]pyrimido[4,5-d]azepine-10-carboxylic acid (I-43) and piperidin-4-yl-carbamic acid tert-butyl ester were converted to {1-[2-(3,4-dimethoxy-phenylamino)-6-oxo-6,7-dihydro-5H-benzo[b]pyrimido[4,5-d]azepine-10-carbonyl]-piperidin-4-yl}-carbamic acid tert-butyl ester, which was subsequently deprotected according to Method K. Purification by C-18 RP LC-MS chromatography afforded I-74 (19%): HRMS Calcd. for C26H28N6O4: 489.2250, Found 489.2253.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07459448B2
Source datasetuspto-grants-2008_12
ORD IDord-570a8bd3910f44a0ae5142c15ed60518
Source noteuspto-grants-2008_12