HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2382042Generated: October 27, 2026
Dimethylformamide → 4-(1-amino-5-fluoro-1H-indol-3-yl)-2-methyl-butan-2-ol
https://huagongshe.com/reaction/2382042
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-(5-fluoro-1H-indol-3-yl)-2-methyl-butan-2-ol | HCID 68559083 | — |
| Product | 4-(1-amino-5-fluoro-1H-indol-3-yl)-2-methyl-butan-2-ol | HCID 68552158 | — |
Reaction Steps
A suspension of NaH (8.1 g, 204 mmol, 60% in mineral oil) in DMF (100 mL) at 0° C. is treated with 4-(5-fluoro-1H-indol-3-yl)-2-methyl-butan-2-ol (3 g, 13.6 mmol) and stirred at 0° C. for 0.5 h. The mixture is treated with HOSA (7.7 g, 68 mmol) portion wise and warmed to rt over 2 h. The mixture is then poured over ice, filtered through a pad of Celite, and extracted with EtOAc (3×100 mL). The combined organic layer is dried (Na2SO4), filtered and concentrated in vacuo. The residue is purified by filtration through a short plug of silica gel to afford 4-(1-amino-5-fluoro-1H-indol-3-yl)-2-methyl-butan-2-ol, which is used in the next step without further purification. MS: 237 (M+H); 1H NMR (300 MHz, CDCl3): δ 7.30 (m, 1H), 7.22 (m, 1H), 6.98 (m, 2H), 4.71 (s, NH2, 2H), 2.75 (m, 2H), 1.86 (m, 2H), 1.31 (s, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08258130B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-070c0434271c486baca24c458aba37cd |
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| Source note | uspto-grants-2012_09 |
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