HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 627685Generated: October 29, 2026
Nitrogen → 2-Pyridinecarboxylic acid, 3-chloro-5-cyano-, 1,1-dimethylethyl ester
https://huagongshe.com/reaction/627685
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Tris(1,1-dimethylethyl)phosphine | HCID 83681 | — |
| Reactant | tert-Butyl 5-bromo-3-chloropyridine-2-carboxylate | HCID 68109709 | — |
| Reactant | HCID 178514179 | HCID 178514179 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Pyridinecarboxylic acid, 3-chloro-5-cyano-, 1,1-dimethylethyl ester | HCID 86728141 | — |
Reaction Steps
A mixture of tert-butyl 5-bromo-3-chloropicolinate (12 g, 41.0 mmol), dicyanozinc (3.37 g, 28.7 mmol), and zinc (0.375 g, 5.74 mmol) were suspended in DMF (82 ml) in round bottom flak. The suspension was purged with N2 and finally Pd2(dba)3 (1.878 g, 2.051 mmol), tri-tert-butylphosphine (6.2 ml, 6.15 mmol) and neat tri-tert-butylphosphine (300 mg), was added under the Ar. The r×n mixture was heated to 95° C. for 3 h. Then another 2.8 g of Pd2(dba)3 and 1.2 g of neat P ligand were added. 3.5 h later, it was cooled to RT and black precipitate was filtered out by filtration. The filtrate was diluted with 150 ml of MTBE. The organic layer was washed with 100 ml of water and brine. It was dried on MgSO4 and concentrated which was carried over to next step directly. MS m/z=261.0/263.0 (M+Na).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09309263B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-284939929b5746f68d90bb24f8fc1ce9 |
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| Source note | uspto-grants-2016_04 |
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