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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2395178Generated: November 1, 2026

Benzyl Alcohol → HCID 86753158, compound

https://huagongshe.com/reaction/2395178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantHCID 86753159HCID 86753159—
SolventDichloromethaneHCID 6344—
ProductHCID 86753158HCID 8675315873.3%

Reaction Steps

A solution of 158 mg (0.77 mmol) of N,N-dicyclohexylcarbodiimide in methylene chloride was added dropwise to an ice-cooled solution of 3.20 mg (0.695 mmol) of (6-tert.-butoxycarbonyl-aminomethyl-3,7-dimethoxy-10-methyl-phenothiazin-4-yl)-acetic acid, 90.2 mg (0.84 mmol) of benzyl alcohol and 20 mg of N,N-dimethylaminopyridine in 2.5 ml of methylene chloride. The reaction mixture was stirred at room temperature overnight and filtered. The filter residue was washed with methylene chloride. The combined filtrates were washed with saturated sodium bicarbonate solution, dried over magnesium sulphate and concentrated. The residue was chromatographed on silica gel with ethyl acetate/hexane (1:4), whereupon, after recrystallization from ethanol and drying, 280 mg (73.3%) of benzyl (6-tert.-butoxycarbonyl-aminomethyl-3,7-dimethoxy-10-methyl-phenothiazin-4-yl)-acetate were obtained as white crystals of m.p. 131°-132°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05811548
Source datasetuspto-grants-1998_09
ORD IDord-a986a16aa17f45cb8d82e6c8234e8b12
Source noteuspto-grants-1998_09