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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1013536Generated: October 25, 2026

Water → Diethyl [({[4-({[2-({[(1,1-dimethylethyl)oxy]carbonyl}amino)-5-(2-thienyl)phenyl]amino}carbonyl)phenyl]methyl}amino)methyl)phosphonate

https://huagongshe.com/reaction/1013536

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiisopropylethylamineHCID 81531—
Reactantdiethyl (aminomethyl)phosphonate oxalate saltHCID 2733594—
ReactantTert-butyl [2-{[4-(bromomethyl)benzoyl]amino}-4-(2-thienyl)phenyl]carbamateHCID 57925962—
SolventDimethylformamideHCID 6228—
ProductDiethyl [({[4-({[2-({[(1,1-dimethylethyl)oxy]carbonyl}amino)-5-(2-thienyl)phenyl]amino}carbonyl)phenyl]methyl}amino)methyl)phosphonateHCID 57925892—

Reaction Steps

1,1-dimethylethyl [2-({[4-(bromomethyl)phenyl]carbonyl}amino)-4-(2-thienyl)phenyl]carbamate (500 mg, 1.026 mmol), diethyl (aminomethyl)phosphonate oxalate (791 mg, 3.08 mmol), and DIPEA (1.254 mL, 7.18 mmol) were stirred in DMF (6 mL) at 50° C. overnight. Room temperature was attained, H2O: was added and the products extracted into EtOAc (×2). The combined organic extracts were washed with brine, dried over MgSO4 and concentrated in vacuo. Purification of the residue by MPLC (0-10% MeOH-EtOAc) gave diethyl [({[4-({[2-({[(1,1-dimethylethyl)oxy]carbonyl}amino)-5-(2-thienyl)phenyl]amino}carbonyl)phenyl]methyl}amino)methyl)phosphonate as a colourless gum. MS: cal'd 574 (MH+), exp 574.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981874B2
Source datasetuspto-grants-2011_07
ORD IDord-bcdfd4dbab7a413b8b2cfc3e04b8015a
Source noteuspto-grants-2011_07