HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1375351Generated: November 1, 2026
3-(Bromomethyl)-1H-indazole, N1-BOC protected → HCID 69431219, compound
https://huagongshe.com/reaction/1375351
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-(Bromomethyl)-1H-indazole, N1-BOC protected | HCID 10804951 | — |
| Reactant | HCID 69427209 | HCID 69427209 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 69431219 | HCID 69431219 | — |
Reaction Steps
To a stirring solution of 1-[2-oxo-2-(2,3,4,5-tetrahydro-1H-1-benzazepin-1-yl)ethyl]-5-phenyl-1H-1,5-benzodiazepine-2,4(3H,5H)-dione (1.0 g, 2.28 mM) in 15 mL DMF at 0° C. was added 1.1 equiv. of 0.5 M solution of KN(TMS)2 in toluene. The resulting solution was stirred 10–30 min, then a solution of tert-butyl 3-(bromomethyl)-1H-indazole-1-carboxylate (0.78 g, 2.5 mM) in 3 mL DMF was added. The resulting solution was stirred 2 h at RT and then quenched with 5 mL of H2O. The reaction mixture was then poured into 50 mL of EtOAc and extracted with H2O (2×50 mL). The organic layer was separated, dried (MgSO4), and the solvents removed in vacuo. The resultant material was purified by silica gel flash column chromatography using hexanes/EtOAc 1/1 providing 1.4 g of white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07169773B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-28e82fab40384f7f98efe96aafefd39a |
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| Source note | uspto-grants-2007_01 |
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