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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1945000Generated: November 2, 2026

Succinic anhydride → HCID 49822297, compound

https://huagongshe.com/reaction/1945000

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSuccinic anhydrideHCID 7922—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 86648192HCID 86648192—
SolventDichloromethaneHCID 6344—
ProductHCID 49822297HCID 4982229786.8%

Reaction Steps

A solution of (R)-ethyl 3-amino-4-(5′-chloro-2′-fluorobiphenyl-4-yl)butanoate hydrochloride (293 mg, 0.777 mmol), succinic anhydride (93 mg, 0.932 mmol) and DIPEA (0.204 mL, 1.165 mmol) in dichloromethane (4 mL) is allowed to stir for 1.5 hours. The reaction is quenched with 1 M aqueous HCl and extracted with dichloromethane. The organic layer is separated and concentrated under reduced pressure. The resulting residue is purified by preparative HPLC using a gradient of 20% MeCN/water (0.1% TFA) to 100% MeCN to give (R)-4-(1-(5′-chloro-2′-fluorobiphenyl-4-yl)-4-ethoxy-4-oxobutan-2-ylamino)-4-oxobutanoic acid (294 mg). HPLC retention time=1.03 minutes (condition B); MS (m+1)=436.2; 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 1.28 (t, J=7.07 Hz, 3H) 2.46-2.58 (m, 4H) 2.64-2.68 (m, 2H) 2.87 (A of ABX, Jab=13.64 Hz, Jax=7.83 Hz, 1H) 2.99 (B of ABX, Jab=13.64 Hz, Jbx=6.57 Hz, 1H) 4.11-4.22 (m, 2H) 4.47-4.56 (m, 1H) 6.60 (br d, J=8.59 Hz, 1H) 7.05-7.10 (m, 1H) 7.23-7.27 (m, 3H) 7.39-7.41 (m, 1H) 7.44-7.46 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394853B2
Source datasetuspto-grants-2013_03
ORD IDord-16a91024256e423bb88972ca299d37c7
Source noteuspto-grants-2013_03