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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2370340Generated: October 30, 2026

Triethylamine → HCID 68228638, compound

https://huagongshe.com/reaction/2370340

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantBoc-L-ValineHCID 83693—
ReactantHCID 87328684HCID 87328684—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 68228638HCID 6822863899.8%

Reaction Steps

A solution of [4-(5-aminomethyl-2-fluoro-phenyl)-piperidin-1-yl]-[7-fluoro-1-(2-methoxy-ethyl)-4-trifluoromethoxy-1H-indol-3-yl]-methanone hydrochloride (0.3 g, 0.55 mmol), BOC-Val-OH (0.143 g, 0.66 mmol), EDCI (0.126 g, 0.66 mmol), HOBT (0.224 g, 1.65 mmol), and Et3N (0.23 ml, 1.65 mmol) in CH2Cl2 (30 mL) was stirred at rt overnight. The reaction mixture was poured into EtOAc and the organic layer washed with 10% citric acid and brine. The organic layer was dried over MgSO4, filtered and concentrated in vacuo to give the crude product. Purification by flash chromatography on SiO2 eluting with 3% MeOH/CH2Cl2 afforded the desired product (0.39 g, 99%). 1H NMR (300 MHz, CDCl3) δ 7.4 (s, 1H), 7.1 (m, 2H), 7.0-6.8 (m, 3H), 6.3 (bs, 1H), 5.0 (bs, 1H), 4.5-4.3 (m, 4H), 3.9 (m, 1H), 3.8 (m, 2H), 3.35 (s, 3H), 3.1 (m, 2H), 2.2 (m, 2H), 2.0-1.6 (m, 6H), 1.4 (s, 9H), 0.9 (m, 6H). MS m/z: [M+H]+=711.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710080B2
Source datasetuspto-grants-2014_04
ORD IDord-4e567e808c514bd5b52b705eebb9d304
Source noteuspto-grants-2014_04