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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 222377Generated: October 30, 2026

Sodium borohydride → HCID 42606679, compound

https://huagongshe.com/reaction/222377

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 42605984HCID 42605984—
SolventDichloromethane methanolHCID 21226129—
ProductHCID 42606679HCID 4260667967%

Reaction Steps

To a suspension of 1-[(3,4-dichlorophenyl)methyl]-N-(5-formyl-1,3-thiazol-2-yl)-5-methyl-1H-1,2,3-triazole-4-carboxamide (Example 5) (1.2 g, 30 mmol), in a mixture of DCM/MeOH, was added sodium borohydride (130 mg). The reaction was stirred at room temperature for 1 hour. After evaporation, the residue was poured in a mixture of water/concentrated HCl solution and extracted with ethyl acetate. A solid was formed and filtered. The filtrate was dried over sodium sulphate and evaporated in vacuo. The combined solids were recrystallised from acetonitrile to give the title compound as a yellow solid (0.8 g, 67%). HRMS calculated for C15H13Cl2N5O2S (M+H)+ 398.0245, found: 398.0205, Rt: 2.59 min. MP: 170.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207204B2
Source datasetuspto-grants-2012_06
ORD IDord-49df11d6d19943acb489c9e01845aa37
Source noteuspto-grants-2012_06