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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167807Generated: November 1, 2026

Sodium Hydroxide → 3-[4-(2-{4-[(2,3-Dihydro-indole-1-carbonyl)-amino]-3-methoxy-phenyl}-acetylamino)-phenyl]-butyric acid

https://huagongshe.com/reaction/1167807

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactantethyl (R) 3-[4-(2-{4-[(2,3-dihydro-indole-1-carbonyl)-amino]-3-methoxy-phenyl}-acetylamino)-phenyl]-butyrateHCID 86585371—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product3-[4-(2-{4-[(2,3-Dihydro-indole-1-carbonyl)-amino]-3-methoxy-phenyl}-acetylamino)-phenyl]-butyric acidHCID 987006986.2%

Reaction Conditions

Temperature50 °C

Reaction Steps

A suspension of ethyl (R) 3-[4-(2-{4-[(2,3-dihydro-indole-1-carbonyl)-amino]-3-methoxy-phenyl}-acetylamino)-phenyl]-butyrate (1.3 g, Reference Example 4) in ethanol (40 mL) and water (15 mL) was treated with sodium hydroxide (5 mL, 1M). After stirring at 50° C. for 3 hours the mixture was evaporated to low bulk and then acidified with hydrochloric acid (1M). The resulting white precipitate was filtered, then washed with water, then with ether, and then dried to give the title compound (1.06 g) as a white powder. HPLC: RT=15.3 minutes (>95% by ELS). MS(ES+): 488(MH+); MS(ES−): 486(M−).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06620832B2
Source datasetuspto-grants-2003_09
ORD IDord-c0cb1b008f944476a6436b4577511ee2
Source noteuspto-grants-2003_09