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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1873283Generated: November 4, 2026

4-Methylmorpholine → methyl N-[(1S)-1-[[(1S,2S)-1-benzyl-3-[[4-(2-tert-butyltetrazol-5-yl)phenyl]methyl-[[(2S)-2-(methoxycarbonylamino)-3,3-dimethyl-butanoyl]amino]amino]-2-hydroxy-propyl]carbamoyl]-2-methyl-propyl]carbamate

https://huagongshe.com/reaction/1873283

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantO-(2-Oxo-1(2H)-pyridyl)-N,N,N',N'-tetramethyluronium TetrafluoroborateHCID 2733204—
Reactant(2S)-2-((methoxycarbonyl)amino)-3-methylbutanoic acidHCID 10942966—
ReactantHCID 22940458HCID 22940458—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Productmethyl N-[(1S)-1-[[(1S,2S)-1-benzyl-3-[[4-(2-tert-butyltetrazol-5-yl)phenyl]methyl-[[(2S)-2-(methoxycarbonylamino)-3,3-dimethyl-butanoyl]amino]amino]-2-hydroxy-propyl]carbamoyl]-2-methyl-propyl]carbamateHCID 467978—

Reaction Steps

Under a nitrogen atmosphere, 54 mg (0.308 mmol) of N-methoxycarbonyl-(L)-valine and 92 mg (0.308 mmol) of TPTU in 1 ml of DMF and 101 μl (0.91 mmol) of NMM are stirred at room temperature for 10 min. 190 mg (0.308 mmol) of 1-[4-(2-tert-butyl-2H-tetrazol-5-yl)-phenyl]-4(S)-hydroxy-5(S)-amino-2-N-[N-methoxycarbonyl-(L)-tert-leucyl]amino-6-phenyl-2-azahexane hydrochloride (Example 34g) in 2 ml of DMF are added thereto and the mixture is stirred at room temperature overnight to complete the reaction. The reaction mixture is diluted with methylene chloride and washed with brine. The aqueous phases are extracted 2× with methylene chloride; the organic phases are filtered through cotton wadding, concentrated by evaporation and chromatographed (SiO2 ; methylene chloride/methanol 30:1): TLC: Rf =0.21 (methylene chloride/methanol 19:1); FAB MS (M+H)+ =738.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06110946
Source datasetuspto-grants-2000_08
ORD IDord-51d03a0ec9844edb91d42c140d4c9d1c
Source noteuspto-grants-2000_08