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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 737060Generated: October 30, 2026

Triethylamine → HCID 58974989, compound

https://huagongshe.com/reaction/737060

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphoniumHCID 124335—
Reactant1-Boc-Azetidine-3-carboxylic acidHCID 2755981—
Reactant(Azetidin-3-yl)methanolHCID 13400658—
ReactantAluminium lithium hydrideHCID 21226445—
Reactant4-(3-Phenyl-indole-1-sulfonyl)-benzoic acidHCID 58975141—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58974989HCID 5897498935.3%

Reaction Steps

Dissolve azetidine-1,3-dicarboxylic acid mono-tert-butyl ester (300 mg, 1.50 mmol.) in THF (5.0 mL) and treat with lithium aluminum hydride (1.0M in ether, 3.0 mL, 3.0 mmol). Stir for 18 hours, quench with 3.0 mL of 1.0M NaOH, dilute with ether, filter through celite and evaporate. Treat the resulting 3-hydroxymethyl-azetidine-1-carboxylic acid tert-butyl ester with 10 mL of trifluoroacetic acid for 20 minutes an evaporate. Use this material without further purification. Combine 4-(3-Phenyl-indole-1-sulfonyl)-benzoic acid (100 mg, 0.26 mmol) and the resulting azetidin-3-yl-methanol in dichloromethane (1.0 mL) and triethylamine (0.100 mL, 0.717 mmol, excess) and add benzotriazol-1-yloxytris(dimethylamino)phosphonium hexfluorophosphate (BOP Reagent) (150 mg, 0.33 mmol, excess) at room temperature. Stir for 30 minutes, evaporate and load entire reaction directly onto pre-packed silica gel column and purify by flash column chromatography (EtOAc/Hexanes) to give 41 mg of (3-Hydroxymethyl-azetidin-1-yl)-[4-(3-phenyl-indole-1-sulfonyl)-phenyl]-methanone as a white solid (35%). LRMS: MH+ 447.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07595339B2
Source datasetuspto-grants-2009_09
ORD IDord-69b27a67a28349cda5c63e723884e0a8
Source noteuspto-grants-2009_09