HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1357278Generated: November 3, 2026
Ammonium Chloride → HCID 178482586, compound
https://huagongshe.com/reaction/1357278
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | 1-methyl-1H-indole-3-carboxylic acid (5-bromo-6-cyanomethoxy-naphthalen-2-ylmethyl)-methyl-amide | HCID 12083574 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178482586 | HCID 178482586 | 84% |
Reaction Steps
A mixture of 1-methyl-1H-indole-3-carboxylic acid (5-bromo-6-cyanomethoxy-naphthalen-2-ylmethyl)-methyl-amide (1.0 g, 2.0 mmol), prepared in the previous step, sodium azide (0.32 g, 6.0 mmol) and ammonium chloride (0.39 g, 6.0 mmol) in 15 mL of DMF was stirred under nitrogen at 100° C. for 6 h. The reaction was partitioned between ethyl acetate and water. The aqueous layer was made basic by the addition of 1 N NaOH. The organic layer was separated and the aqueous layer extracted five times with ethyl acetate. The aqueous layer was then acidified with 1N HCl. After 2 h a white solid had precipitated from solution. The solid was collected by filtration and dried under reduced pressure to give the title compound (0.8460 g, 84%) as an off-white solid, mp 227-228° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06589970B2 |
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| Source dataset | uspto-grants-2003_07 |
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| ORD ID | ord-f258b715facd431d81a5f5e4808e22e5 |
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| Source note | uspto-grants-2003_07 |
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