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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615783Generated: November 2, 2026

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

https://huagongshe.com/reaction/1615783

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant(R)-tert-butyl 5-oxo-4-(2-oxo-2-((R)-2'-oxo-1,1',2',3-tetrahydrospiro[inden-2,3'-pyrrolo-[2,3-b]pyridin]-5-ylamino)ethyl)-3-phenyl-8,11-dioxa-1,4-diazaspiro[5.6]-dodecane-1-carboxylateHCID 49842606—
SolventMethanolHCID 887—
ProductN-((R)-2'-oxo-1,1',2',3-tetrahydrospiro[inden-2,3'-pyrrolo[2,3-b]pyridin]-5-yl)-2-((R)-5-oxo-3-phenyl-8,11-dioxa-1,4-diazaspiro[5.6]dodecan-4-yl)acetamideHCID 49842495—

Reaction Conditions

Temperature50 °C

Reaction Steps

0.27 g (0.41 mmol) (R)-tert-butyl 5-oxo-4-(2-oxo-2-((R)-2′-oxo-1,1′,2′,3-tetrahydrospiro[inden-2,3′-pyrrolo-[2,3-b]pyridin]-5-ylamino)ethyl)-3-phenyl-8,11-dioxa-1,4-diazaspiro[5.6]-dodecane-1-carboxylate in 5 ml of methanol were combined with 10 ml of a 1.25 M methanolic hydrochloric acid and stirred for 3 h at 50° C. The reaction mixture was concentrated by rotary evaporation and neutralised 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-5bd392d9cb7a4a70a22d22a32ff091c4
Source noteuspto-grants-2014_07