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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1168532Generated: October 25, 2026

1-Boc-1-methylhydrazine → ethyl 2-(2,3-difluoro-5-iodobenzoyl)-3-[2-methyl-2-[(2-methylpropan-2-yl)oxycarbonyl]hydrazinyl]prop-2-enoate

https://huagongshe.com/reaction/1168532

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Boc-1-methylhydrazineHCID 3748280—
ReactantEthyl 2-(2,3-Difluoro-5-iodobenzoyl)-3-ethoxy-2-propenoateHCID 69879816—
Solventtert-ButanolHCID 6386—
Productethyl 2-(2,3-difluoro-5-iodobenzoyl)-3-[2-methyl-2-[(2-methylpropan-2-yl)oxycarbonyl]hydrazinyl]prop-2-enoateHCID 17847213992.2%

Reaction Steps

A solution of ethyl 2-(2,3-difluoro-5-iodobenzoyl)-3-ethoxy-2-propenoate (Preparation 21, 7.80 g) in tert-butanol (40 mL) is cooled with a cold water bath and a solution of tert-butyl 1-methylhydrazinecarboxylate (2.92 g) in tert-butanol (4 mL) is added. The cooling bath is removed, the mixture is stirred for 5 min at ambient temperature, and then is heated in an oil bath at 45° C. for 40 min. The reaction mixture is poured into 100 mL of crushed ice/water and extracted two times with ethyl acetate. The combined organic layers are dried (Na2SO4) and concentrated in vacuo. The crude product is purified by chromatography, using 300 g of silica gel, packed and eluted with EtOAc/heptane (1/3), to afford 8.95 g (92%) of the title compound as a yellow oily foam. Physical characteristics: 1H NMR (CDCl3) δ8.14, 8.07, 7.59-7.49, 7.46-7.41, 4.07, 3.30, 3.26, 1.50, 1.09, 0.97; MS (ESI+) m/z 511 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06624159B2
Source datasetuspto-grants-2003_09
ORD IDord-64a0e742feee401781161d683297aaa4
Source noteuspto-grants-2003_09