HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 42494Generated: October 26, 2026
tert-Butanol → Tert-butyl (5-cyano-6-methoxy-4-methylpyridin-2-yl)carbamate
https://huagongshe.com/reaction/42494
Participants
| Role | Name | HCID | Charge |
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| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | 5-Cyano-6-methoxy-4-methylpicolinic acid | HCID 67467527 | — |
| Product | Tert-butyl (5-cyano-6-methoxy-4-methylpyridin-2-yl)carbamate | HCID 86677356 | 59.4% |
Reaction Steps
To a stirred solution of 5-cyano-6-methoxy-4-methylpicolinic acid (0.75 g, 3.90 mmol) in tert-butanol (25 mL) was added triethylamine (0.7 mL, 5.02 mmol). After the reaction became clear DPPA (1 mL, 4.64 mmol) was added dropwise over 5 minutes. The reaction was slowly heated to 100° C. and stirred for 4 hr. The reaction was cooled to RT and evaporated to dryness under vacuum. Purified by silica gel chromatography (Analogix, SF25-60 g, 0 to 20% EtOAc in hexanes) to give, after trituration and filtration from hexanes, the product tert-butyl (5-cyano-6-methoxy-4-methylpyridin-2-yl)carbamate (0.61 g, 2.317 mmol, 59.4% yield) as a white solid. 1H NMR (400 MHz, DMSO-d6) δ 10.20 (s, 1H), 7.44 (s, 1H), 3.91 (s, 3H), 2.40 (s, 3H), 1.48 (s, 9H). MS (ES)+m/e 264.0 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08536179B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-e50e1554872749b9ac0ecdf60ad262f8 |
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| Source note | uspto-grants-2013_09 |
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