HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 457771Generated: October 29, 2026
Dimethylformamide → HCID 69419456, compound
https://huagongshe.com/reaction/457771
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Bromomethyl acetate | HCID 68536 | — |
| Reactant | HCID 54483006 | HCID 54483006 | — |
| Product | HCID 69419456 | HCID 69419456 | 92% |
Reaction Steps
1.95 g (6.13 mmol) of 4-benzylpiperidinyl indole-5-carboxamide was dissolved in 30 mL dry DMF and was treated with 320 mg (8 mmol, 60% suspension in oil) sodium hydride for 30 minutes. The reaction mixture was cooled to 0° C. and 1.225 g (8 mmol) bromomethylacetate was added and stirring continued for 1 h at 0° C. The ice-bath was removed and stirring continued for another 6 h at room temperature. The reaction was quenched by the addition of sat. ammonium chloride solution, diluted with water and extracted with dichloromethane. The extract was dried, evaporated and the residue purified by column chromatography on silica gel eluting with ethylacetate-hexane (25–35% ethylacetate) to yield 2.2 g (92%) of the desired product. MS: M+, 390; M+−1, 389. 1HNMR (CDCl3): □ 7.7 (s, 1H); 7.35–7.1 (m, 8H); 6.6 (s, 1H); 5.1 (s, 2H); 3.75 (s, 3H); 3.0–2.7 (br, m, 4H); 2.6 (d, 2H); 1.9–1.2 9m, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07189739B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-d850aed22aac45e5bf14c1786e7a1ba3 |
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| Source note | uspto-grants-2007_03 |
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