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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1158483Generated: November 3, 2026

2-Mercaptoethanol → HCID 68618327, compound

https://huagongshe.com/reaction/1158483

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MercaptoethanolHCID 1567—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant((3S*,4R*)-1-benzyl-4-{[isopropyl-(2-nitro-benzenesulfonyl)-amino]-methyl}-pyrrolidin-3-ylmethyl)-isopropyl-carbamic acid tert-butyl esterHCID 68616510—
SolventAcetonitrileHCID 6342—
ProductHCID 68618327HCID 68618327—

Reaction Steps

A solution of ((3S*,4R*)-1-benzyl-4-{[isopropyl-(2-nitro-benzenesulfonyl)-amino]-methyl}-pyrrolidin-3-ylmethyl)-isopropyl-carbamic acid tert-butyl ester (8.9 g, 23.02 mmol), 2-mercaptoethanol (0.81 mL, 11.60 mmol), and DBU (0.79 mL, 5.27 mmol) in CH3CN (10 mL) is stirred for 2 h at room temperature. The mixture is concentrated and then diluted with Et2O and H2O. The organic layer is separated, and the aqueous phase is extracted 3 times with Et2O. The combined organic extracts are dried (MgSO4), and the solvent is concentrated to give the title compound which is used without further purification in the next step. TLC, Rf (AcOEt)=0.61. MS (LC-MS): 404.3 [M+H]+; tR (HPLC, C18 column, 10-100% CH3CN/H2O/5 min, 100% CH3CN/2.5 min, CH3CN and H2O containing 0.1% TFA, flow: 1.5 mL/min): 4.45 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807709B2
Source datasetuspto-grants-2010_10
ORD IDord-90a9452c074e4e5ba9eab8d2f2a3bc30
Source noteuspto-grants-2010_10