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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2042701Generated: October 26, 2026

tert-butyl N-(4-aminobutyl)carbamate → HCID 67074748, compound

https://huagongshe.com/reaction/2042701

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl N-(4-aminobutyl)carbamateHCID 4351—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2-(Di-tert-butylphosphino)biphenylHCID 2734215—
ReactantTert-butyl 4-(4-(1-(3-bromophenyl)cyclopropylamino)-6-(2,2,2-trifluoroethoxy)-1,3,5-triazin-2-ylamino)benzoateHCID 67074285—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventDichloromethaneHCID 6344—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 67074748HCID 6707474828%

Reaction Conditions

Temperature85 °C

Reaction Steps

To a mixture of tert-butyl 4-(4-(1-(3-bromophenyl)cyclopropylamino)-6-(2,2,2-trifluoroethoxy)-1,3,5-triazin-2-ylamino)benzoate (116 mg, 0.2 mmol),tert-butyl 4-aminobutylcarbamate (37.7 mg, 0.200 mmol), 2-(Di-t-butylphosphino)biphenyl (0.020 mmol), Pd2(dba)3 (18.31 mg, 0.020 mmol), K3PO4 (34.8 mg, 0.200 mmol) in a microwave tube in DME (Volume: 2 mL) was stirred for 3 h at 85° C. The reaction mixture was diluted with CH2Cl2, filtrated through a celite plug washing with CH2Cl2, concentrated to give a residue that was purified by Biotage eluting with 20%-50% ethyl acetate in hexane to give 38 mg (28%) of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586584B2
Source datasetuspto-grants-2013_11
ORD IDord-bee6d08c77b1468a8b7d702ce630eda3
Source noteuspto-grants-2013_11