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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1935335Generated: November 1, 2026

P-Toluic Acid → HCID 54306168, compound

https://huagongshe.com/reaction/1935335

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-Toluic AcidHCID 7470—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantHCID 69941088HCID 69941088—
SolventDimethylformamideHCID 6228—
ProductHCID 54306168HCID 5430616840.4%

Reaction Conditions

Temperature75 °C

Reaction Steps

4—Methylbenzoic acid (22 mg, 0.16 mmol) and 1,1′-carbonyldiimidazole (27 mg, 0.17 mmol) were dissolved in dry N,N-dimethylformamide (2 mL) and stirred at 75° C. for 1 h. The reaction mixture was cooled to room temperature and a solution of (S)-3-amino-8-methyl-5-(methylpiperazin-1-yl)-3,4-dihydro-2H-1-benzopyran (40 mg, 0.15 mmol) dissolved in dry N,N-dimethylformamide (4 mL) was added. The reaction mixture was stirred at room temperature for 4 days and the solvent was evaporated in vacuo. The crude material was partitioned between methylene chloride (40 mL) and water (10 mL). The organic phase was washed with water (10 mL) and brine (5 mL) and dried (MgSO4). The solvent was evaporated in vacuo giving 48 mg of a crude product. Purification by preparative TLC on silica using chloroform/ethanol (saturated with ammonia) (15:1) as the eluent afforded 23 mg (40% yield) of the title compound as a white solid: mp 191-192° C.; EIMS (70eV) m/z (relative intensity) 379 (100, M+); [α]21D−7° (c 0.10, chloroform).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06387899B1
Source datasetuspto-grants-2002_05
ORD IDord-0996b9f50df0489fa3707c681bfc8a31
Source noteuspto-grants-2002_05