HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108360Generated: October 30, 2026
Water → (2S)-2-amino-3-(4-amino-5-{[3-({[(2,4-dichlorophenyl)amino]carbonyl}amino)phenyl]carbonyl}pyrrolo[2,1-f][1,2,4]triazin-7-yl)propanoic acid
https://huagongshe.com/reaction/2108360

Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Methyl 2-((tert-butoxycarbonyl)amino)-3-iodopropanoate | HCID 5051066 | — |
| Reactant | 1-{3-[(4-Amino-7-bromopyrrolo[2,1-f][1,2,4]triazin-5-yl)carbonyl]phenyl}-3-(2,4-dichlorophenyl)urea | HCID 16739790 | — |
| Reactant | Chlorotrimethylsilane 1,2-dibromoethane | HCID 86760839 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+) | HCID 178418228 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | (2S)-2-amino-3-(4-amino-5-{[3-({[(2,4-dichlorophenyl)amino]carbonyl}amino)phenyl]carbonyl}pyrrolo[2,1-f][1,2,4]triazin-7-yl)propanoic acid | HCID 57629493 | 4.8% |
Reaction Steps
A mixture of zinc dust (300 mg) in dimethylacetamide (DMA) (0.3 mL) at 50° C. was treated with a solution of chlorotrimethylsilane/1,2-dibromoethane (7/5 v/v, 0.04 mL) and the reaction was stirred at room temperature for 30 minutes. A solution of methyl 2-(tert-butoxycarbonylamino)-3-iodopropanoate (247 mg, 0.75 mmol) in DMA (1 mL) was slowly added and the reaction was stirred for 40 minutes. This mixture was added to a mixture of 95G (35 mg), PdCl2(dppf)2 (7 mg), and CuI (10 mg) in DMA (0.8 mL). The reaction was heated to 80° C. for 18 hours. Water was added and the solid precipitate was collected by filtration. The solid was treated with 33% HBr/AcOH and then concentrate. The residue was dissolved in THF/MeOH and water and treated with LiOH and stirred at room temperature for two hours. The reaction mixture was neutralized with trifluoroacetic acid and purified by preparative reversed phase HPLC to afford the desired product (1.7 mg). Compound 103 had an analytical HPLC retention time=2.906 min. (Chromolith SpeedROD column 4.6×50 mm, 10-90% aqueous methanol over 4 minutes containing 0.1% TFA, 4 ml/min, monitoring at 220 nm) and a LC/MS M++1=528+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07514435B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-fda981b455f54606b3ddeb265fe1492f |
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| Source note | uspto-grants-2009_04 |
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