Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Bromoacetyl chloride | HCID 89602 | — |
| Reactant | Potassium Bromide | HCID 253877 | — |
| Reactant | HCID 9970997 | HCID 9970997 | — |
| Solvent | Butanol acetic acid water | HCID 22056973 | — |
| Product | HCID 10052502 | HCID 10052502 | — |
Reaction Steps
To a solution of 503 mg (1.42 mmol) of 9 .2HCl in 15 mL of dry dimethyl formamide were added sequentially, 533 μL (6.59 mmol) of pyridine and 282 μL (3.42 mmol) of bromoacetyl chloride. After allowing the mixture to stir at room temperature for 6 hours, the precipitated product was filtered off and rinsed with water and then rinsed with ethanol: 393 mg (53%) yield; mp 308°-310° C.; TLC (n-butanol/acetic acid/water [5:2:3]), Rf =0.58; IR (KBr pellet) 3380, 3278, 1681, 1638, 1551, 1472, 1411, 1325, 1238, 1047 cm-1 ; 1H NMR (dimethyl-d6 sulfoxide) δ9.72 (2H, s, 2- and 5-acetamido N(H), 7.87 (2H, brs, 3- and 6-carbamyl proton), 4.22 (4H, s, methylenes), 3.65 (6H, s, methoxys), 2.70 (6H, d, J=4.6 Hz, 3- and 6-carbamyl methyl); mass spectrum (EI mode) m/z 522, 524 and 526 (P+ for the 79Br, 79Br; 79Br, 81Br; 81Br, 81Br combinations, respectively, at an intensity ratio of 1:2:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05639881 |
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| Source dataset | uspto-grants-1997_06 |
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| ORD ID | ord-9034fde3a9164a89af163dfcf8e9706e |
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| Source note | uspto-grants-1997_06 |
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