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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1845213Generated: October 26, 2026

Diisopropylethylamine → (R)-Ethyl 5-(3-hydroxypyrrolidine-1-carbonyl)-4'-methylbiphenyl-3-carboxylate

https://huagongshe.com/reaction/1845213

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant(R)-3-PyrrolidinolHCID 2759337—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Reactant5-(Ethoxycarbonyl)-4'-methylbiphenyl-3-carboxylic acidHCID 58187957—
SolventDichloromethaneHCID 6344—
Product(R)-Ethyl 5-(3-hydroxypyrrolidine-1-carbonyl)-4'-methylbiphenyl-3-carboxylateHCID 58188314—

Reaction Steps

To a mixture of 5-(ethoxycarbonyl)-4′-methylbiphenyl-3-carboxylic acid (1.50 g, 5.28 mmol), N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (2.0 g, 10 mmol), 1-hydroxybenzotriazole hydrate (0.404 g, 2.64 mmol), and CH2Cl2 (30 mL) were added (R)-3-hydroxypyrrolidine (0.92 g, 10 mmol) and N,N-diisopropylethylamine (1.8 mL, 10 mmol). The mixture was stirred at room temperature overnight, and then diluted with CH2Cl2 (100 mL), washed with aq. NaHCO3, brine, dried (Na2SO4), and concentrated in vacuo. The residue was purified by silica gel column (100% EtOAc) to afford a white foam. LC-MS: 354.2 [M+1]+; 1H NMR (400 MHz, CDCl3): 8.32 (s, 1H), 8.16 and 8.12 (bs, 1H), 7.92 (m, 1H), 7.53 (d, 2H, J=7.6 Hz), 7.28 (d, 2H, J=8.4 Hz), 4.63 and 4.49 (bs, 1H), 4.41 (q, 2H, J=7.2 Hz), 3.95-3.40 (m, 4H), 2.41 (s, 3H), 2.20-1.90 (m, 2H), 1.41 (t, 3H, J=7.2 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946439B2
Source datasetuspto-grants-2015_02
ORD IDord-cd806b11768c4545b032a1d0a02f310a
Source noteuspto-grants-2015_02