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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1158343Generated: November 2, 2026

(3S,4S)-3-({isopropyl-[4-methoxy-3-(3-methoxy-propoxy)-benzoyl]-amino}-methyl)-4-[(methyl-phenylacetyl-amino)-methyl]-pyrrolidine-1-carboxylic acid tert-butyl ester → (3R,4R)-3-({Isopropyl-[4-methoxy-3-(3-methoxy-propoxy)-benzoyl]-amino}-methyl)-4-[(methyl-phenylacetyl-amino)-methyl]-pyrrolidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1158343

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3S,4S)-3-({isopropyl-[4-methoxy-3-(3-methoxy-propoxy)-benzoyl]-amino}-methyl)-4-[(methyl-phenylacetyl-amino)-methyl]-pyrrolidine-1-carboxylic acid tert-butyl esterHCID 68616928—
SolventEthanolHCID 702—
Product(3R,4R)-3-({Isopropyl-[4-methoxy-3-(3-methoxy-propoxy)-benzoyl]-amino}-methyl)-4-[(methyl-phenylacetyl-amino)-methyl]-pyrrolidine-1-carboxylic acid tert-butyl esterHCID 59512485—

Reaction Steps

Racemic (3R*,4R*)-3-({isopropyl-[4-methoxy-3-(3-methoxy-propoxy)-benzoyl]-amino}-methyl)-4-[(methyl-phenylacetyl-amino)-methyl]-pyrrolidine-1-carboxylic acid tert-butyl ester is separated into the single enantiomers by preparative chiral HPLC on a Chiralpak AD-H column (4.6×250 mm, 5 μM particle size; flow rate 1 mL/min, UV=210 nM, injection=1.7 g in 5 mL ethanol and using ethanol as the eluent to give the enantiomerically pure title compound: tR (HPLC, Chiralpak AD-H, HPLC 250×4.6 mm, ethanol, flow: 0.5 ml/min): 26.46 min; and (3S,4S)-3-({isopropyl-[4-methoxy-3-(3-methoxy-propoxy)-benzoyl]-amino}-methyl)-4-[(methyl-phenylacetyl-amino)-methyl]-pyrrolidine-1-carboxylic acid tert-butyl ester: tR (HPLC, Chiralpak AD-H, HPLC 250×4.6 mm, ethanol, flow: 0.5 ml/min): 13.53 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807709B2
Source datasetuspto-grants-2010_10
ORD IDord-b9fc6f99bb294a2a8a5f9e4f3c0e9b2b
Source noteuspto-grants-2010_10