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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587064Generated: October 31, 2026

1,3-Thiazole-5-carbaldehyde → Methyl 7-[4-(2-butoxyethoxy)phenyl]-1-(1,3-thiazol-5-ylmethyl)-2,3-dihydro-1-benzazepine-4-carboxylate

https://huagongshe.com/reaction/587064

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Thiazole-5-carbaldehydeHCID 2773577—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantMethyl 7-[4-(2-butoxyethoxy)phenyl]-1-benzazepine-4-carboxylateHCID 69749802—
Solvent1,2-DichloroethaneHCID 11—
ProductMethyl 7-[4-(2-butoxyethoxy)phenyl]-1-(1,3-thiazol-5-ylmethyl)-2,3-dihydro-1-benzazepine-4-carboxylateHCID 2232900679.9%

Reaction Steps

In 1,2-dichloroethane (15 ml) was dissolved methyl 7-[4-(2-butoxyethoxy)phenyl]-1-benzazepine-4-carboxylate (0.50 g). To the solution were added 1,3-thiazole-5-carbaldehyde 10.43 g) and sodium triacetoxyborohydride (0.80 g), and the mixture was stirred at room temperature for 24 hours. To the mixture was added sodium triacetoxyborohydride (0.27 g), and the mixture was stirred for 6 hours. The solvent was removed under reduced pressure, the resulting residue was added to water, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine and dried with magnesium sulfate. The solvent was removed under reduced pressure, and the resulting residue was purified with silica gel column chromatography (hexane/ethyl acetate=3/2→2/3) to give methyl 7-[4-(2-butoxyethoxy)phenyl]-1-(1,3-thiazol-5-ylmethyl)-2,3-dihydro-1-benzazepine-4-carboxylate (0.50 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06936602B1
Source datasetuspto-grants-2005_08
ORD IDord-20fab3757f764e6cb93121b37c4e138d
Source noteuspto-grants-2005_08