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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 324370Generated: October 30, 2026

Triethylamine → HCID 22004611, compound

https://huagongshe.com/reaction/324370

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAcetic acid 10-acetoxymethyl-anthracen-9-ylmethyl esterHCID 613145—
ReactantHCID 22004591HCID 22004591—
SolventDichloromethaneHCID 6344—
ProductHCID 22004611HCID 22004611—

Reaction Steps

A solution of 3-{benzyl-[6-methyl-3-methylsulfanyl-1-(2,4,6-trichlorophenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-yl]amino}-propanol (80 mg, 0.148 mmol) in 1 ml of methylene chloride was treated with acetic anhydrous (38 mg, 0.37 mmol) and triethyl amine (38 mg, 0.37 mmol) and stirred at room temperature for 15 hours. The mixture was quenched with water and a few drops of dilute HCl and extracted with ethyl acetate. The organic layer was neutralized with aqueous sodium bicarbonate and washed with brine, separated, dried and concentrated to give the title compound as an oil. The oil was purified through silica gel column chromatography using chloroform as eluent to give 57 mg of the title compound as a white glass form. 1H NMR (CDCl3): 2.0(s,3H, 2.03(m,2H), 2.45(s,3H), 2.60(s,3H), 3.74(t,2H), 4.10(t,2H), 5.1(s,2H), 7.2-7.4(m,5H), 7.50(s,2H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06218397B1
Source datasetuspto-grants-2001_04
ORD IDord-e5aff774fbef4629ac9e92e91bfe9088
Source noteuspto-grants-2001_04