HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1801458Generated: October 30, 2026
Potassium Carbonate → [3-(6-Methoxy-3-nitro-pyridin-2-ylamino)-propyl]-carbamic acid tert-butyl ester
https://huagongshe.com/reaction/1801458
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | tert-Butyl (3-aminopropyl)carbamate | HCID 2735700 | — |
| Reactant | 2-Chloro-6-methoxy-3-nitropyridine | HCID 2795029 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | [3-(6-Methoxy-3-nitro-pyridin-2-ylamino)-propyl]-carbamic acid tert-butyl ester | HCID 68631911 | 96.5% |
Reaction Steps
A mixture of 2-chloro-6-methoxy-3-nitropyridine (5.9 g; commercial), N-(tert-butoxycarbonyl)-1,3-propanediamine (4.48 g; commercial) and K2CO3 (3.55 g) in MeCN (90 mL) and DMF (25 mL) was heated at 40° C. for 30 min. The reaction mixture was filtered and the filtrate was evaporated under reduced pressure. The residue was taken up in EA, sequentially washed with water and brine and evaporated under reduced pressure, affording 8.1 g (96% yield) of a crude yellow solid which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08349826B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-556912d0069e4d7fb161e5c767c13ca7 |
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| Source note | uspto-grants-2013_01 |
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