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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 251323Generated: October 31, 2026

Diisopropylethylamine → Benzyl (2s,3s)-2-(2-(2-(3-ethylureido)-5-(trifluoromethyl)benzamido)acetamido)-3-hydroxyhex-4-ynylcarbamate

https://huagongshe.com/reaction/251323

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
Reactant2-(3-Ethylureido)-5-(trifluoromethyl)benzoic acidHCID 22268752—
Reactant(2S,3S)-2-(2-aminoacetamido)-3-hydroxyhex-4-ynylcarbamateHCID 86596716—
SolventDichloromethaneHCID 6344—
ProductBenzyl (2s,3s)-2-(2-(2-(3-ethylureido)-5-(trifluoromethyl)benzamido)acetamido)-3-hydroxyhex-4-ynylcarbamateHCID 91439354—

Reaction Steps

A solution of benzyl (2S,3S)-2-[2-(tert-butoxycarbonylamino)acetamido]-3-hydroxyhex-4-ynylcarbamate (315 mg; see WO-02/50019 for preparation) in methylene chloride (6 mL) was cooled to 0° C. and charged with trifluoroacetic acid (2 mL). The mixture was allowed to warm to RT and stirred for 45 min before being concentrated in vacuo. The residue was dissolved in methylene chloride and the resultant solution concentrated; this was repeated twice more to afford the TFA salt of (2S,3S)-2-(2-aminoacetamido)-3-hydroxyhex-4-ynylcarbamate, MS found: (M+H)+=320.6. A solution of this amine in CH2Cl2 (8 mL) was charged successively with N,N-diisopropylethylamine (0.66 mL), 2-(3-ethylureido)-5-(trifluoromethyl)benzoic acid (208 mg, see WO-02/50019), and BOP (399 mg). The reaction was stirred for 14 h at RT before being partitioned between EtOAc and water. The organic phase was washed with sat. NH4Cl, water, and brine before being dried (Na2SO4), filtered, and concentrated in vacuo. Flash chromatography provided benzyl (2S,3S)-2-(2-(2-(3-ethylureido)-5-(trifluoromethyl)benzamido)acetamido)-3-hydroxyhex-4-ynylcarbamate (167 mg). MS found: (M+H)+=578.5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07863333B2
Source datasetuspto-grants-2011_01
ORD IDord-63e783807a564d0693095c45c13c34f4
Source noteuspto-grants-2011_01