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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2075772Generated: October 25, 2026

Acetic Acid → HCID 178452458, compound

https://huagongshe.com/reaction/2075772

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDiisopropylcarbodiimideHCID 12734—
ReactantLithium hydroxide, monohydrateHCID 168937—
Reactant(3S)-4-(tert-Butoxycarbonyl)morpholine-3-carboxylic acidHCID 1512537—
Reactant2-[4-(4-Amino-phenylethynyl)-1H-pyrazol-3-yl]-4-chloro-phenolHCID 178507548—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 178452458HCID 17845245871.4%

Reaction Steps

To a solution of compound 24A (930 mg, 3.0 mmol) and (S)-morpholine-3,4-dicarboxylic acid 4-tert-butyl ester (19A, 2.09 g, 9.0 mmol) in anhydrous dichloromethane (20 mL) was added N,N′-diisopropylcarbodiimide (DIPC, 1.4 mL, 9.0 mmol). The reaction mixture was stirred at rt overnight. Solvent was removed. To the residua were added THF (20 mL) and methanol (20 mL) and a solution of LiOH.H2O (1.0 g, 23.84 mmol) in water (10 mL). The mixture was stirred at rt for 2 h. It was then neutralized with acetic acid (1.36 mL, 23.84 mmol). The mixture was diluted with ethyl acetate (˜100 mL), washed with brine, and dried over sodium sulfate. It was filtered, concentrated and filtered again to remove diisopropylurea. The filtrate was purified with silica column chromatography eluting with dichloromethane/ethyl acetate (v/v 5/1, 3/1, 2/1, 1/1) to provide the title compound (28A, 1.12 g) as a yellowish solid in 71.3% yield. LCMS (ESI) m/z 587.15 (MNa+), 521.05 (MH+), 421.06; HPLC: tR=5.32 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07923004B2
Source datasetuspto-grants-2011_04
ORD IDord-adbb3e7842b04fda9aaad5fd9a282c7c
Source noteuspto-grants-2011_04