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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1628356Generated: November 1, 2026

Hydrochloric Acid → HCID 178453818, compound

https://huagongshe.com/reaction/1628356

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 86762557HCID 86762557—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178453818HCID 17845381834.4%

Reaction Steps

4-(tert-Butoxycarbonylamino-{[1-(4-chloro-phenyl)-cyclopropylmethyl]-carbamoyl}-methyl)-cyclohexanecarboxylic acid propyl ester (2-2) (1.77 g, 0.0035 mol, 1 eq) was dissolved in MeOH (20 mL) and THF (6 mL). NaOH (0.42 g, 0.0105 mol, 3 eq) in H2O (2 mL) was added. The reaction mixture was stirred at RT and monitored by TLC and LC/MS. After stirring at RT for 20 hours, the reaction mixture was diluted with H2O. The pH was adjusted to pH=3 with 10% HCl while cooling with ice-H2O bath. The aqueous was extracted with EtOAc (3×60 mL). The combined EtOAc was washed with brine. After drying over Na2SO4 and filtration, the filtrate was concentrated under vacuum to dryness. The crude product was purified on silica gel column, eluted with 2% MeOH/CH2Cl2 to give trans-4-(tert-Butoxycarbonylamino-{[1-(4-chloro-phenyl)-cyclopropylmethyl]-carbamoyl}-methyl)-cyclohexanecarboxylic acid 0.56 g (2-3) (34.4%). 1H NMR (DMSO-d6) data is depicted in FIG. 19.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785648B1
Source datasetuspto-grants-2014_07
ORD IDord-8a9e490175904b7d83ff55944e0e2672
Source noteuspto-grants-2014_07