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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1849986Generated: October 29, 2026

4-Methylmorpholine → Benzyl [(1R)-2-({(2R)-2-[(tert-butoxycarbonyl)amino]-3-phenylpropyl}amino)-1-methyl-2-oxoethyl]carbamate

https://huagongshe.com/reaction/1849986

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantBOC-D-alanineHCID 637606—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Reactant(R)-Benzyl 1-amino-3-phenylpropan-2-ylcarbamateHCID 69740353—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductBenzyl [(1R)-2-({(2R)-2-[(tert-butoxycarbonyl)amino]-3-phenylpropyl}amino)-1-methyl-2-oxoethyl]carbamateHCID 86717649104.5%

Reaction Steps

Benzyl-[(1R)-2-amino-1-benzylethyl]carbamate (described in J. Med. Chem., 2010, p 106; 200 mg, 0.71 mmol) and N—BOC-D-alanine (134 mg, 0.71 mmol) were added to a stirred solution of 1-(3-dimethylaminopropyl)-3-ethyl-carbodiimide hydrochloride salt (163 mg, 0.85 mmol), 1-hydroxybenzotriazole monohydrate (115 mg, 0.75 mmol) and N-methylmorpholine (72 mg, 0.71 mmol) in DMF (3 mL) at room temperature under a nitrogen atmosphere. After 16 h the mixture was treated with 8 mL of ethyl acetate (creating a suspension) and washed with 12 mL of a 10% aqueous citric acid solution, 12 mL of water, 12 mL of a 3% aqueous solution of sodium bicarbonate, and another 10 mL of a saturated aqueous brine solution. The organic layer was dried over sodium sulfate and evaporated under reduced pressure to give 338 mg (93%) of a white foam of the title compound, which was used with no further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957025B2
Source datasetuspto-grants-2015_02
ORD IDord-5a1b8a05696c4932a99af03a4221e4c3
Source noteuspto-grants-2015_02