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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1985510Generated: November 2, 2026

Isoamyl Nitrite → (S)-Diethyl 2-((4-(acetoxymethyl)-7-bromo-1H-indazol-5-yl)methyl)succinate

https://huagongshe.com/reaction/1985510

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsoamyl NitriteHCID 8053—
ReactantPotassium AcetateHCID 517044—
Reactant2-(S)-(2-Acetoxymethyl-4-amino-5-bromo-3-methyl-benzyl)-succinic acid diethyl esterHCID 59731880—
SolventAcetic AcidHCID 176—
SolventTolueneHCID 1140—
Product(S)-Diethyl 2-((4-(acetoxymethyl)-7-bromo-1H-indazol-5-yl)methyl)succinateHCID 5973185477%

Reaction Conditions

Temperature0 °C

Reaction Steps

Isoamyl nitrite (2.3 mL, 17 mmol), was added drop-wise to an ice cold solution of 2-(S)-(2-Acetoxymethyl-4-amino-5-bromo-3-methyl-benzyl)-succinic acid diethyl ester (7.14 g, 16 mmol) in 5% acetic acid in toluene (280 mL). Mixture stirred at 0° C. for 40 minutes. Potassium acetate (4.00 g, 41 mmol) was added to the mixture. Mixture was slowly warmed to room temperature. Reaction was stirred at room temperature for 14 hours. Mixture was washed twice with water and once with brine. Organic was dried (magnesium sulfate) filtered and concentrated. Silica gel chromatography (ethyl acetate-hexanes) afforded the desired product in 77% yield as an amber oil. MS m/e (M+H)+=455.0, 457.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07544680B2
Source datasetuspto-grants-2009_06
ORD IDord-1640aaa87d1549588d3471311bfb5e72
Source noteuspto-grants-2009_06