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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507138Generated: October 30, 2026

Ethyl Acetate → HCID 11578234, compound

https://huagongshe.com/reaction/507138

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant2-DimethylaminopyridineHCID 21885—
ReactantSodium hydrideHCID 24758—
Reactanttert-butyl N-(2-hydroxyethyl)carbamateHCID 2733206—
ReactantHCID 59432299HCID 59432299—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 11578234HCID 11578234—

Reaction Steps

To a solution of (S)-5-[(3,5-Bis-trifluoromethyl-benzyl)-(2-methyl-2H-tetrazol-5-yl)-amino]-7-methyl-8-trifluoromethyl-2,3,4,5-tetrahydro-benzo[b]azepine-1-carbonyl chloride (0.08 mmol) in dimethylformamide (3 mL), add (2-Hydroxy-ethyl)-carbamic acid tert-butyl ester (0.24 mmol) and dimethylaminopyridine (0.08 mmol). Next, add sodium hydride (0.24 mmol) and stir at room temperature for 0.5 h. Quench the reaction with water (15 mL) and dilute with ethyl acetate (10 mL). Separate the organic phase and wash the aqueous with ethyl acetate (2×10 mL). Dry the combined organics over sodium sulfate, filter, and remove solvent under vacuum. Dissolve the crude 5-[(3,5-Bis-trifluoromethyl-benzyl)-(2-methyl-2H-tetrazol-5-yl)-amino]-7-methyl-8-trifluoromethyl-2,3,4,5-tetrahydro-benzo[b]azepine-1-carboxylic acid 2-tert-butoxycarbonylamino-ethyl ester intermediate in dichloromethane (5 mL) and add trifluoroacetic acid (2 mL). After stirring for 1 h, quench the reaction with concentrated sodium carbonate (5 mL). Dilute the reaction with dichloromethane (10 mL) and water (10 mL). Separate the organic phase and wash the aqueous with dichloromethane (2×10 mL). Dry the combined organics over sodium sulfate, filter, and remove the solvent under vacuum. Chromatograph the product over silica gel, eluting with methanol/dichloromethane (0-5%), to afford the title compound as a colorless foam. MS (ES+): 640 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786108B2
Source datasetuspto-grants-2010_08
ORD IDord-0b68b06da7bd44818acbb43d33ed3590
Source noteuspto-grants-2010_08