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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1527432Generated: November 4, 2026

Diisopropylethylamine → (1R,3S,5S)-3-(2-Fluoro-3-trifluoromethoxy-phenylcarbamoyl)-5-(tetrahydro-pyran-2-yloxymethyl)-2-aza-bicyclo[3.1.0]hexane-2-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1527432

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1-Chloro-N,N-2-trimethylpropenylamineHCID 640792—
Reactant2-Fluoro-3-(trifluoromethoxy)anilineHCID 25210503—
Reactant(1R,3S,5S)-5-(Tetrahydro-pyran-2-yloxymethyl)-2-aza-bicyclo[3.1.0]hexane-2,3-dicarboxylic acid 2-tert-butyl esterHCID 68284002—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product(1R,3S,5S)-3-(2-Fluoro-3-trifluoromethoxy-phenylcarbamoyl)-5-(tetrahydro-pyran-2-yloxymethyl)-2-aza-bicyclo[3.1.0]hexane-2-carboxylic acid tert-butyl esterHCID 68283049—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of (1R,3S,5S)-5-(tetrahydro-pyran-2-yloxymethyl)-2-aza-bicyclo[3.1.0]hexane-2,3-dicarboxylic acid 2-tert-butyl ester (100 mg, 0.29 mmol) in dry CH2Cl2 (1 mL) under argon at 0° C. was added 1-chloro-N,N,2-trimethylpropenylamine (58 μL, 0.44 mmol) and the reaction mixture was stirred at 0° C. for 1.5 h. 2-Fluoro-3-(trifluoromethoxy)aniline (86 mg, 0.44 mmol) was added, followed by DIPEA (100 μL, 0.59 mmol) and the mixture was stirred at RT overnight. Then poured into water and extracted with CH2Cl2 (×2), the organics were dried (Na2SO4), filtered and concentrated. The crude residue was purified by flash column chromatography on silica gel (eluent: c-hexane to c-hexane/EtOAc 85:15). TLC, Rf (c-hexane/EtOAc 2:1)=0.45; MS (UPLC/MS): 519.3 [M+H]+, 536.3 [M+NH4]+, 517.4 [M−H]−, 563.3 [M−HCOO]−; tR (HPLC conditions f): 2.51 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09085555B2
Source datasetuspto-grants-2015_07
ORD IDord-f13495b3515d4ccf98c61e0c693ae1b1
Source noteuspto-grants-2015_07