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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 267075Generated: November 2, 2026

Triethylamine → N-(2(S)-(t-butoxycarbonylamino)-3(S)-methylpentyl)glycine methyl ester

https://huagongshe.com/reaction/267075

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantGlycine methyl ester hydrochlorideHCID 122755—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant1,1-Dimethylethyl N-((1S,2S)-1-formyl-2-methylbutyl)carbamateHCID 11390272—
Solvent1,2-DichloroethaneHCID 11—
SolventDimethylformamideHCID 6228—
ProductN-(2(S)-(t-butoxycarbonylamino)-3(S)-methylpentyl)glycine methyl esterHCID 10755806—

Reaction Conditions

Temperature0 °C

Reaction Steps

Glycine methyl ester hydrochloride (4.41 g, 0.035 mol) was dissolved in 1,2-dichloroethane (50 mL) and DMF (5 mL) and treated with 3A molecular sieves (10 g) and N-t-butoxycarbonyl-isoleucinal (6.3 g, 0.029 mol) with stirring at 0° C. Sodium triacetoxyborohydride (9.27 g, 0.044 mol) was added, and the pH of the mixture was adjusted to 6 with triethylamine (3 mL, 0.022 mol). After stirring for 18 h the mixture was filtered, concentrated to a small volume and partitioned between EtOAc and water. The aqueous layer was extracted with EtOAc (2×50 mL). The combined organic phase was washed with aqueous saturated NaHCO3 solution, brine, and dried (Na2SO4). Filtration and concentration afforded a residue which was purified by flash chromatography (SiO2, EtOAc:hexane, 1:3) to give (6).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05652257
Source datasetuspto-grants-1997_07
ORD IDord-cddb864aa6ef4947b6c960da79180f6a
Source noteuspto-grants-1997_07