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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2373421Generated: October 30, 2026

tert-butyl N-(4-aminobutyl)carbamate → HCID 59851078, compound

https://huagongshe.com/reaction/2373421

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl N-(4-aminobutyl)carbamateHCID 4351—
ReactantHCID 59851270HCID 59851270—
ReactantHCID 59851365HCID 59851365—
ProductHCID 59851078HCID 59851078—

Reaction Steps

In a manner similar to that described Method N, 2-(3,4-dimethoxy-phenylamino)-6-oxo-6,7-dihydro-5H-benzo[b]pyrimido[4,5-d]azepine-9-carboxylic acid (I-53) and tert-butyl 4-aminobutylcarbamate were converted to (2-{[2-(3,4-dimethoxy-phenylamino)-6-oxo-6,7-dihydro-5H-benzo[b]pyrimido[4,5-d]azepine-9-carbonyl]-amino}-ethyl)-carbamic acid tert-butyl ester, which was subsequently deprotected (Method K) to give I-73 (25%): HRMS Calcd. for C25H28N6O4: 477.2250, Found 477.2250.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07459448B2
Source datasetuspto-grants-2008_12
ORD IDord-5b7aa2f6fbeb4e259ca02cb4dda8a4f7
Source noteuspto-grants-2008_12