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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1741435Generated: November 1, 2026

Sulfuric acid magnesium salt (1:1) → (2S,9S)-7-Benzyl-2-[(tert-butoxycarbonyl)amino]-10-chloro-9-hydroxy-7-azadecanoic Acid, tert-Butyl Ester

https://huagongshe.com/reaction/1741435

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
Reactant(+)-EpichlorohydrinHCID 149428—
ReactantNepsilonBenzyl-Nalpha-BOC-L-Lysine tert-Butyl EsterHCID 10786720—
SolventMethanolHCID 887—
Product(2S,9S)-7-Benzyl-2-[(tert-butoxycarbonyl)amino]-10-chloro-9-hydroxy-7-azadecanoic Acid, tert-Butyl EsterHCID 1060092677%

Reaction Steps

A mixture of Nε -benzyl-Nα -BOC-L-lysine t-butyl ester (4) (16.0 g, 40.76 mmol), CH3OH (40 ml), (S)-(+)-epichlorohydrin (4.17 g, 45.0 mmol) and anhydrous MgSO4 (5.33 g. 44.28 mmol) was stirred under N2 for three days. The solids were filtered off and washed with CH3OH. The filtrate was concentrated at room temperature to give a yellow oil. The resulting oil was purified by flash chromatography on silica gel (66% hexane/ethyl acetate) to give 13.23 g of (5) (77%) as a colorless oil. 1H NMR (C6D6) δ7.18 (m, 5H), 5.00 (br d, 1H), 4.40 (m, 1H), 3.62 (m, 1H), 3.40-3.10 (m, 4H), 2.20-2.00 (m, 4H), 1.63 (m, 1H), 1.40 (s, 9H), 1.31 (s, 9H), 1.20 (m, 2H). 13C NMR (C6D6) δ171.7, 155.2, 138.8, 128.8, 127.9, 127.0, 80.8, 78.8, 67.7, 58.8, 57.2, 53.9, 53.7, 47.3, 32.5, 28.0, 27.5, 26.3, 22.8. HRMS m/z calcd. for C25H42ClN2O5 485.2782, found 485.2775. [α]25D +5.3° (c=1.00, CHCl3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05973113
Source datasetuspto-grants-1999_10
ORD IDord-cb6d2c23a64048858607271730d08b0c
Source noteuspto-grants-1999_10