Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1527550Generated: November 4, 2026

Sodium Hydroxide → HCID 68284110, compound

https://huagongshe.com/reaction/1527550

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 68283474HCID 68283474—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68284110HCID 68284110—

Reaction Steps

To a solution of (1-carbamoyl-3-{[(1R,3S,5R)-3-(3-chloro-2-fluoro-benzylcarbamoyl)-2-aza-bicyclo[3.1.0]hexane-2-carbonyl]-amino}-1H-indol-5-yloxy)-acetic acid methyl ester Example 133 (85 mg, 0.145 mmol) in THF (1.2 mL) and H2O (120 μL) was added NaOH 1N (290 μL, 0.29 mmol) and the reaction mixture was stirred at RT for 20 min. The crude was directly purified using trimethylaminopropyl cartridge (Mega Bond Elut-SAX, 1 g from Varian) pre-washed with CH3CN (10 mL) and the compound was released with 10 mL of HCl 0.1N in CH3CN. The resulting solution was concentrated and purified by preparative HPLC (Waters Sunfire, C18-ODB, 5 μm, 19×50 mm, eluent: 20% to 100% CH3CN in H2O in 15 min, CH3CN and H2O containing 0.1% HCOOH, flow: 20 mL/min) to give the desired material after lyophilization of the purified fractions. MS (UPLC-MS): 544.3/546.3 [M+H]+, 566.4/568.3 [M+Na]+, 542.3/544.4 [M−H]−; tR (HPLC conditions f): 1.72 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09085555B2
Source datasetuspto-grants-2015_07
ORD IDord-45c0b1ee06fe44f897cfd0fe4921cb37
Source noteuspto-grants-2015_07