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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 859112Generated: October 31, 2026

tert-butyl N-(4-aminobutyl)carbamate → HCID 86595104, compound

https://huagongshe.com/reaction/859112

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl N-(4-aminobutyl)carbamateHCID 4351—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 69630855HCID 69630855—
SolventAcetonitrileHCID 6342—
ProductHCID 86595104HCID 86595104—

Reaction Steps

Diisopropylethylamine (0.1 mL, 0.6 mmol) and 4-t-butoxycarbonylamino-butylamine (25 mg, 1.4 mmol) are added to a solution of N-[3-ethoxycarbonyl-phenyl]-4-[2-chloro-4-trifluoromethyl-5-thiazolyl]-2-pyrimidineamine (52 mg, 0.12 mmol) in 50 mL anhydrous acetonitrile. The mixture is then heated to reflux overnight. The reaction is stopped, cooled to room temperature and concentrated. Water (30 mL) is added and the reaction mixture is extracted with ethyl acetate (3×100 mL). The combined organic layers are dried over MgSO4, filtered and concentrated. The residue is used in the next step without further purification; ESI-MS (m/z): 567.2 (M++H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07151096B2
Source datasetuspto-grants-2006_12
ORD IDord-ad043861f79b425bac8734e650daf8f5
Source noteuspto-grants-2006_12