HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2039790Generated: November 2, 2026
Dimethylformamide dimethyl acetal → HCID 25094556, compound
https://huagongshe.com/reaction/2039790
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide dimethyl acetal | HCID 78373 | — |
| Reactant | HCID 86646641 | HCID 86646641 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 25094556 | HCID 25094556 | — |
Reaction Steps
A mixture of 3-[(adamantan-1-ylmethyl)carbamoyl]-1-[2-(3-cyanophenyl)-2-oxoethyl]-2-methylpyridinium bromide (400 mg, 0.81 mmol) and N,N-dimethylformamide dimethyl acetal (0.22 mL, 1.62 mmol) in DMF (2.0 mL) is stirred at 110° C. for 3 h. The mixture is concentrated in vacuo and purified by column chromatography (gradient from CH2Cl2 to 10% EtOAc/CH2Cl2) to give the title compound as a yellow solid. 1H NMR (400 MHz, DMSO-d6) δ 9.91 (1H, d), 8.53 (1H, t), 8.15 (1H, m), 8.05 (2H, m), 7.74 (1H, t), 7.66 (1H, dd), 7.44 (1H, d), 7.22 (1H, t), 6.95 (1H, d), 3.01 (2H, d), 1.93 (3H, s), 1.63 (6H, m), 1.52 (6H, s). Mass spec. (438.19, M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08580812B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-73a7ba1a4c454af0b250fd91d6c4361b |
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| Source note | uspto-grants-2013_11 |
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