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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167828Generated: October 30, 2026

HCID 16637187, compound → HCID 22993961, compound

https://huagongshe.com/reaction/1167828

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 16637187HCID 16637187—
ReactantHCID 54012078HCID 54012078—
SolventMethanolHCID 887—
ProductHCID 22993961HCID 2299396139%

Reaction Steps

A solution of 4-amino-2-(trityl-amino)-thiazole-5-carbothioic acid amide (304 mg, 0.73 mmol) and N-(3-Bromoacetyl-phenyl)-benzamide (300 mg, 0.94 mmol) in MeOH (30 ml) was stirred at room temperature overnight. The solvent was removed in vacuo and the residue was dissolved in EtOAc (100 ml). The EtOAc solution was washed with a saturated aqueous solution of NaHCO3 (3×25 ml). The organic layer was separated, dried over MgSO4, and concentrated. Purification of the residue was achieved by silica gel chromatography (75% EtOAc/DCM) providing N-[3-(2′,4′-diamino-[2,5′]bithiazolyl-4-yl)-phenyl]-benzamide (110 mg, 39% yield). mp 159-163° C. (decomp). 1H NMR (CD3OD): δ 8.33 (s, 1H), 8.00-7.97 (m, 2H), 7.75-7.71 (m, 2H), 7.64-7.52 (m, 3H), 7.43 (t, J=7.74 Hz, 1H), 7.33 (s, 1H). FABMS Calcd for C19H15N5OS2: 394.0796. Found: 394.0802.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06620828B2
Source datasetuspto-grants-2003_09
ORD IDord-9a0b8e7357c8499b8075ba8c460503a5
Source noteuspto-grants-2003_09