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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2395138Generated: November 3, 2026

Hydrochloric Acid → HCID 86753165, compound

https://huagongshe.com/reaction/2395138

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPyridineHCID 1049—
ReactantGlutaric anhydrideHCID 7940—
ReactantHCID 131720845HCID 131720845—
SolventTolueneHCID 1140—
ProductHCID 86753165HCID 8675316571.1%

Reaction Steps

A mixture of 360 mg (0.67 mmol) of benzyl (6-tert.-butoxycarbonyl-aminomethyl-3,7-dimethoxy-phenothiazin-4-yl)acetate, 91.7 mg (0.80 mmol) of glutaric anhydride and. 63.7 mg (0.80 mmol) of pyridine in 5 ml of toluene was treated with 10 mg of N,N-dimethylaminopyridine. The mixture was heated to 110° under argon for 48 hours and then poured into ice-water, whereupon the mixture was acidified with 1N hydrochloric acid and exhaustively extracted with methylene chloride. The organic phase was dried over magnesium sulphate and concentrated. The residue was chromatographed on silica gel with chloroform/methanol (9:1), whereupon 310 mg (71%) of 5-(4-benzyloxycarbonylmethyl-6-tert.-butoxycarbonyl-aminomethyl-3,7-dimethoxy-phenothiazin-10yl)-5-oxo-pentanoic acid were obtained as a white solid of m.p. 65°-68°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05811389
Source datasetuspto-grants-1998_09
ORD IDord-cb7149414fd947e6bae552c2ca8bf79e
Source noteuspto-grants-1998_09