HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 494711Generated: October 27, 2026
Sodium Azide → 6-Azido-4-(4-bromo-2-chlorophenylamino)nicotinic acid tert-butyl ester
https://huagongshe.com/reaction/494711
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | 4-(4-Bromo-2-chlorophenylamino)-6-chloronicotinic acid tert-butyl ester | HCID 86596778 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 6-Azido-4-(4-bromo-2-chlorophenylamino)nicotinic acid tert-butyl ester | HCID 86596779 | 43% |
Reaction Steps
Sodium azide (1.51 g, 23.2 mmol) was added to a suspension of 4-(4-bromo-2-chlorophenylamino)-6-chloronicotinic acid tert-butyl ester (40) (3.23 g, 7.73 mmol) in DMF (60 mL). The reaction mixture was heated to 80° C. and stirred for 16 hours. After cooling to room temperature, the reaction was diluted with EtOAc and washed with water, saturated NaHCO3 and brine. The organic layer was dried (Na2SO4) and concentrated. Purification by flash column chromatography using the Biotage system (CH2Cl2) (repeated) provided the desired product (41) (1.41 g, 43%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07538120B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-92f24da971fd48c0aa2e829f42208fbe |
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| Source note | uspto-grants-2009_05 |
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