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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1424073Generated: November 2, 2026

1-(4-Bromophenyl)cyclopropane-1-carbohydrazide → (8R)-3-[1-(4-Bromophenyl)cyclopropyl]-8-({[t-butyl(dimethyl)silyl]oxy}methyl)-8-methyl-5,6,8,9-tetrahydro[1,2,4]triazolo[4,3-d][1,4]thiazepine

https://huagongshe.com/reaction/1424073

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Bromophenyl)cyclopropane-1-carbohydrazideHCID 43244609—
Reactant(7R)-7-({[t-Butyl(dimethyl)silyl]oxy}methyl)-7-methyl-5-(methylthio)-2,3,6,7-tetrahydro-1,4-thiazepineHCID 71466071—
Solvent1-ButanolHCID 263—
Product(8R)-3-[1-(4-Bromophenyl)cyclopropyl]-8-({[t-butyl(dimethyl)silyl]oxy}methyl)-8-methyl-5,6,8,9-tetrahydro[1,2,4]triazolo[4,3-d][1,4]thiazepineHCID 8671292086.9%

Reaction Conditions

Temperature140 °C

Reaction Steps

The compound (1.02 g, 3.19 mmol) obtained in Example 4-1) and the compound (0.81 g, 3.19 mmol) obtained in Example 16-3) were dissolved in 1-butanol (5 mL), and the mixture was stirred at 140° C. for 6 h under a nitrogen atmosphere. The reaction mixture was cooled to room temperature, then the solvent was distilled off, and the obtained residue was purified by silica gel column chromatography (elution solvent: methanol/ethyl acetate=0% to 20%) to obtain the title compound (1.41 g, 85%) in a white solid form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927536B2
Source datasetuspto-grants-2015_01
ORD IDord-a3c28dfdf2914af083e81189be5d6444
Source noteuspto-grants-2015_01