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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1433048Generated: October 25, 2026

Diisopropylethylamine → 2-[2-Benzyloxycarbonylamino-propylamino]-pentanoic acid methyl ester

https://huagongshe.com/reaction/1433048

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantBenzyl 1-methyl-2-oxoethylcarbamateHCID 563116—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactantmethyl (2S)-2-aminopentanoate hydrochlorideHCID 14118488—
CatalystAcetic AcidHCID 176—
CatalystZincchlorideHCID 3007855—
SolventMethanolHCID 887—
Product2-[2-Benzyloxycarbonylamino-propylamino]-pentanoic acid methyl esterHCID 6902799538.6%

Reaction Steps

To a solution of [1-methyl-2-oxo-ethyl]-carbamic acid benzyl ester (12.3 g, 69 mmol) and norvaline methylester hydrochloride (11.6 g, 69 mmol) in MeOH (300 mL) is added diisopropyl ethyl amine (9.4 g, 73 mmol) and 2 drops of acetic acid. After 10 min., ZnCl2 (9.46 g, 69 mmol) and sodium cyanoborohydride (8.72 g, 14 mmol) is added. The solution is stirred at ambient for 16 h. The solution is then concentrated. The residue is dissolved in EtOAc and 1N KHSO4. The organic layer is washed with 1N KHSO4, H2O, and sat. NaCl. The organic layer is dried over MgSO4, filtered and concentrated. The crude product is purified by column chromatograghy eluting with a gradient of 20% EtOAc/hexane to 40% EtOAc/hexanes. The title compound (8.6 gm, 26.6 mmol) is obtained as a foam. MS (ion spray) m/z 323, (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612075B2
Source datasetuspto-grants-2009_11
ORD IDord-aa4a4c2600c048e99a1e0176bd434d07
Source noteuspto-grants-2009_11