HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 991492Generated: November 2, 2026
Ammonium Chloride → HCID 178432683, compound
https://huagongshe.com/reaction/991492
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 4-Iodo-1-tritylimidazole | HCID 618252 | — |
| Reactant | N,2-Dimethyl-3-pyridinecarboxamide | HCID 12833322 | — |
| Reactant | HCID 178418443 | HCID 178418443 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178432683 | HCID 178432683 | — |
Reaction Steps
To a solution of 4-iodo-1-tritylimidazole (6.88 g, 15.8 mmol) in 65 mL anhydrous dichloromethane was added 6.3 mL of a solution of ethyl magnesium bromide (3.0 M, 18.9 mmol) in diethyl ether under argon. The reaction mixture was stirred for 2.5 h, and then a solution of N-methoxy, N-methyl-2-methylnicotinamide (2.84 g, 15.8 mmol) was added. After 5 days of stirring, the reaction mixture was poured into saturated aqueous ammonium chloride solution (125 mL). The layers were separated, and the aqueous layer was extracted twice with dichloromethane (50 mL). The organic extracts were combined, dried (Na2SO4), and concentrated to provide a red-orange foam which was purified on flash silica gel (1% methanol-chloroform to 2% methanol-chloroform) to provide the desired product as 5.56 g (82%) of a golden-brown foam. MS (PB-NH3), m/z 430 (MH+). 1H NMR (CDCl3) δ 2.63 (s, 3H), 7.02-7.16 (m, 7H), 7.19 (dd, J=7.8, 5.1 Hz, 1H), 7.28-7.41 (m, 8H), 7.49 (d, J=0.9 Hz, 1H), 7.70 (d, J=0.9 Hz, 1H), 7.96 (dd, J=7.9, 1.2 Hz, 1H), 8.57 (dd, J=7.9, 4.9 Hz, 1H.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06465486B1 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-731ae8ac3bcb48a9b540a308ec397f93 |
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| Source note | uspto-grants-2002_10 |
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