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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2204276Generated: October 31, 2026

Triethylamine → HCID 58551224, compound

https://huagongshe.com/reaction/2204276

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-Methylspiro[chromeno[4,3-c]pyrazole-4,4'-piperidine]HCID 58550738—
ReactantBenzoic acid, 3-formyl-4-(1-methylethoxy)-HCID 58551403—
SolventDichloromethaneHCID 6344—
ProductHCID 58551224HCID 5855122434.6%

Reaction Steps

1-Methylspiro[chromeno[4,3-c]pyrazole-4,4′-piperidine] (250 mg, 0.76 mmol), 3-formyl-4-isopropoxy-benzoic acid (160 mg, 0.76 mmol), EDCI (160 mg, 0.84 mmol), and Et3N (430 μL, 3.1 mmol) were combined in dichloromethane (7.1 mL) and the reaction mixture was stirred at room temperature for 48 hours. The reaction mixture was washed with a 1 M HCl (×2), a saturated aqueous solution of NaHCO3 (×2) and a saturated aqueous solution of NaCl. The organic layer was dried over Na2SO4, filtered and the solvent was evaporated under reduced pressure. The crude product was purified by column chromatography on silica gel (0-30% ethyl acetate in dichloromethane) to yield 2-isopropoxy-5-(1-methylspiro[chromeno[4,3-c]pyrazole-4,4′-piperidine]-1′-carbonyl)benzaldehyde (117 mg, 34%) as a light yellow solid. ESI-MS m/z calc. 445.2, found 446.3 (M+1)+; Retention time: 1.74 minutes (3 min run).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365588B2
Source datasetuspto-grants-2016_06
ORD IDord-a8da5b8b21e44f9b89aab4f789902dfe
Source noteuspto-grants-2016_06