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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615781Generated: November 3, 2026

Hydrochloric Acid → N-(5-chloro-2'-oxo-1,1',2',3-tetrahydrospiro[inden-2,3'-pyrrolo[2,3-b]pyridin]-6-yl)-2-((R)-3-(3,5-difluorophenyl)-5-oxo-8,11-dioxa-1,4-diazaspiro[5.6]dodecan-4-yl)acetamide

https://huagongshe.com/reaction/1615781

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant(3R)-tert-butyl 4-(2-(5-chloro-2'-oxo-1,1',2',3-tetrahydrospiro[inden-2,3'-pyrrolo[2,3-b]pyridin]-6-ylamino)-2-oxoethyl)-3-(3,5-difluorophenyl)-5-oxo-8,11-dioxa-1,4-diazaspiro[5.6]dodecane-1-carboxylateHCID 68154278—
ProductN-(5-chloro-2'-oxo-1,1',2',3-tetrahydrospiro[inden-2,3'-pyrrolo[2,3-b]pyridin]-6-yl)-2-((R)-3-(3,5-difluorophenyl)-5-oxo-8,11-dioxa-1,4-diazaspiro[5.6]dodecan-4-yl)acetamideHCID 49842605—

Reaction Conditions

Temperature50 °C

Reaction Steps

40 mg (0.06 mmol) (3R)-tert-butyl 4-(2-(5-chloro-2′-oxo-1,1′,2′,3-tetrahydrospiro[inden-2,3′-pyrrolo[2,3-b]pyridin]-6-ylamino)-2-oxoethyl)-3-(3,5-difluorophenyl)-5-oxo-8,11-dioxa-1,4-diazaspiro[5.6]dodecane-1-carboxylate were combined with 30 ml of a 1N methanolic hydrochloric acid solution and stirred for 1 h at 50° C. The reaction mixture was concentrated by rotary evaporation. The residue was taken up in water and adjusted to pH=8 with saturated NaHCO3 solution. The precipitate formed was suction filtered, washed with water and dried.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765763B2
Source datasetuspto-grants-2014_07
ORD IDord-c77505e0855d44599df9cc27cdf5fb27
Source noteuspto-grants-2014_07