HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972880Generated: October 31, 2026
7-Bromopyrrolo[2,1-f][1,2,4]triazin-4-amine → HCID 58529670, compound
https://huagongshe.com/reaction/1972880
Participants
| Role | Name | HCID | Charge |
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| Reactant | 7-Bromopyrrolo[2,1-f][1,2,4]triazin-4-amine | HCID 42281383 | — |
| Reactant | tert-Butyl 7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydroisoquinoline-2(1H)-carboxylate | HCID 53302321 | — |
| Catalyst | Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+) | HCID 178418228 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Solvent | Sodium Carbonate | HCID 10340 | — |
| Product | HCID 58529670 | HCID 58529670 | 98.7% |
Reaction Steps
To a solution of 7-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butylester (4 g, 11 mmol) and 7-bromo-pyrrolo[2,1-f][1,2,4]triazin-4-ylamine (1.3 g, 6.1 mmol) in DME (133 mL) and 2 N Na2CO3 solution (26 mL) was added Pd(dppf)Cl2 (452 mg, 0.6 mmol). The reaction mixture was degassed with N2 for 15 min. The mixture was heated to 80° C. for 23 h. The reaction mixture was filtered through a pad of Celite® and the filtrate was concentrated in vacuo. The crude residue was purified by Biotage® to provide 2.20 g (55%) of the desired product. 1H NMR (300 MHz, DMSO-d6) δ 7.9 (m, 2 H), 7.85 (d, 1 H), 7.2 (d, 1 H), 7.0 (d, 2 H), 4.5 (s, 2 H), 3.5 (t, 2 H), 2.8 (t, 2 H) 1.4 (s, 9 H); ES-MS m/z 366.05 [M+H]+, HPLC RT (min) 2.64.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08431695B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-19a956df8eff4eddb8f0b2215892d47c |
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| Source note | uspto-grants-2013_04 |
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