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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 493690Generated: October 25, 2026

2,3-Difluorobenzaldehyde → tert-Butyl 1-(2,3-difluorobenzyl)-5-oxo-4-(2,2,2-trifluoroethyl)-1,4-diazepan-6-ylcarbamate

https://huagongshe.com/reaction/493690

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-DifluorobenzaldehydeHCID 137664—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactanttert-Butyl 7-oxo-1-(2,2,2-trifluoroethyl)-1,4-diazepan-6-ylcarbamateHCID 66939478—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
Producttert-Butyl 1-(2,3-difluorobenzyl)-5-oxo-4-(2,2,2-trifluoroethyl)-1,4-diazepan-6-ylcarbamateHCID 6843300788.6%

Reaction Steps

A mixture of tert-butyl 7-oxo-1-(2,2,2-trifluoroethyl)-1,4-diazepan-6-ylcarbamate (51 mg, 0.16 mmol), 2,3-difluorobenzaldehyde (0.053 mL, 0.49 mmol), and sodium cyanoborohydride (31 mg, 0.49 mmol) in methanol (5 mL) was adjusted to pH 4 with acetic acid. After 0.5 h, saturated aqueous sodium bicarbonate was added and the mixture was extracted with dichloromethane (3×). The combined organic extracts were dried over magnesium sulfate, filtered, and concentrated. Purification by silica gel chromatography [100% dichloromethane→95% dichloromethane/5% (10% ammonium hydroxide/methanol)] gave the title compound (62 mg). MS 438 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07534784B2
Source datasetuspto-grants-2009_05
ORD IDord-9ef6d48f4c254d5cbc30c5b37e507d76
Source noteuspto-grants-2009_05