HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167830Generated: November 3, 2026
Trifluoroacetic acid → HCID 22994087, compound
https://huagongshe.com/reaction/1167830
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 53963301 | HCID 53963301 | — |
| Reactant | HCID 54012078 | HCID 54012078 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22994087 | HCID 22994087 | 36% |
Reaction Steps
The title compound was prepared as follows. To a solution of 1.07 g (3.0 mmol) of 4-amino-2-(trityl-amino)-thiazole-5-carbothioic acid amide (prepared analogously to the starting material described in step (ii) of Example A(1)) dissolved in DMF (12 mL), was added 5-chloro-thiophene-2-carboxylic acid (3-bromoacetyl-phenyl)-amide. After 15 minutes, the reaction was diluted with MeOH (12 mL), treated with TFA (4 mL), and stirred overnight. The resulting solution was concentrated in vacuo, diluted with ethyl acetate, extracted with 1M NaHCO3, extracted with brine, dried over MgSO4, concentrated, and purified by flash chromatography (gradient elution: 5% CH3CN/CH2Cl2 to 30% CH3CN/CH2Cl2), giving 0.47 g (36% yield) of N-[3-(2′,4′-diamino-[2,5′]bithiazolyl-4-yl)phenyl]-5-chloro-thiophene-2-carboxamide.
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-aed50fd97ca04dfdafd03158fefd8d5d |
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| Source note | uspto-grants-2003_09 |
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