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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615775Generated: October 30, 2026

1-Hydroxybenzotriazole → HCID 49842383, compound

https://huagongshe.com/reaction/1615775

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant(R)-5-Amino-1,3-dihydrospiro[indene-2,3'-pyrrolo[2,3-b]pyridin]-2'(1'H)-oneHCID 53260812—
ReactantHCID 68154442HCID 68154442—
SolventDimethylformamideHCID 6228—
ProductHCID 49842383HCID 49842383—

Reaction Conditions

Temperature50 °C

Reaction Steps

100 mg (0.21 mmol) 2-((3S)-4-(tert-butoxycarbonyl)-3-(cycloheptylmethyl)-6-(3,5-difluorophenyl)-2-oxopiperazin-1-yl)ethanoic acid, 58 mg (0.23 mmol) (R)-5-amino-1,3-dihydrospiro[inden-2,3′-pyrrol[2,3-b]pyridin]-2′(1′H)-one, 56 mg (0.29 mmol) 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide-hydrochloride, 39 mg (0.29 mmol) HOBT, 0.03 ml (0.23 mmol) TEA and 1.50 ml DMF were stirred overnight at RT. The mixture was concentrated by rotary evaporation. The residue was combined with 15 ml of a 1.25M methanolic hydrochloric acid and stirred for 2 h at 50° C. The diastereomers were separated by RP-HPLC. The fractions containing the product were lyophilised.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765763B2
Source datasetuspto-grants-2014_07
ORD IDord-b086998e28244384bd9596f53cd74a8c
Source noteuspto-grants-2014_07