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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1511568Generated: November 3, 2026

Triethylamine → HCID 45380175, compound

https://huagongshe.com/reaction/1511568

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAmmonium ChlorideHCID 25517—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant(2S,4R)-4-Hydroxypyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl esterHCID 2734883—
Reactant1,2,3,4-Tetrahydroisoquinolin-8-olHCID 13635214—
SolventDimethylformamideHCID 6228—
ProductHCID 45380175HCID 4538017569%

Reaction Conditions

Temperature50 °C

Reaction Steps

Carbonyldiimidazole (0.176 g, 1.086 mmol) was added to a stirred, room temperature solution of DMF (5 mL) and N-Boc-trans-4-hydroxy-L-proline methyl ester (0.21 g, 0.87 mmol) and the mixture was stirred 45 min. 8-Hydroxy-1,2,3,4-tetrahydroisoquinoline (0.20 g, 0.87 mmol) and Et3N (0.18 g, 1.74 mmol) were added and the resulting solution was heated at 50° C. for 2 h. The reaction mixture was poured into aqueous saturated NH4Cl and extracted with EtOAc, dried over Na2SO4 and concentrated to an oil. The residue was purified by column chromatography on silica gel (gradient elution, 10 to 80% EtOAc in hexanes) to give 1-tert-butyl 2-methyl (2S,4R)-4-{[(8-hydroxy-3,4-dihydroisoquinolin-2(1H)-yl)carbonyl]oxy}pyrrolidine-1,2-dicarboxylate (0.25 g, 0.60 mmol, 69% yield) as a colorless foam after evaporation of solvent. LRMS (ESI) m/z 321.3 [((M-Boc)+H)+; calcd for C16H21N2O5: 321.4].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08216999B2
Source datasetuspto-grants-2012_07
ORD IDord-a47accc833944299b8d19d75e6466d0d
Source noteuspto-grants-2012_07