HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167828Generated: October 30, 2026
HCID 16637187, compound → HCID 22993961, compound
https://huagongshe.com/reaction/1167828
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 16637187 | HCID 16637187 | — |
| Reactant | HCID 54012078 | HCID 54012078 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 22993961 | HCID 22993961 | 39% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06620828B2 |
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| Source dataset | uspto-grants-2003_09 |
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| ORD ID | ord-9a0b8e7357c8499b8075ba8c460503a5 |
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| Source note | uspto-grants-2003_09 |
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