HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2374994Generated: November 1, 2026
Cyclopropanecarbonyl chloride → HCID 58711982, compound
https://huagongshe.com/reaction/2374994
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclopropanecarbonyl chloride | HCID 77637 | — |
| Reactant | HCID 58711967 | HCID 58711967 | — |
| Reactant | 6-(1-aminoethyl)-N-[4-(methyloxy)phenyl]-1,2,4-triazin-3-amine | HCID 58711999 | — |
| Product | HCID 58711982 | HCID 58711982 | — |
Reaction Steps
In a similar manner as described for Intermediate 59, using 6-(1-aminoethyl)-N-[4-(methyloxy)phenyl]-1,2,4-triazin-3-amine (Intermediate 47) (100 mg, 0.41 mmol), and cyclopropanecarbonyl chloride (0.043 mL, 0.45 mmol), except the reaction was stirred for 1 h at −78° C., to afford N-[1-(3-{[4-(methyloxy)phenyl]amino}-1,2,4-triazin-6-yl)ethyl]cyclopropanecarboxamide (110 mg) as a yellow solid. 1H NMR (DMSO): δ9.87 (s, 1H), 8.64 (d, J=8.0 HZ, 1H), 8.35 (s, 1H), 7.62 (d, J=8.6 Hz, 2H), 6.91 (d, J=8.6 Hz, 2H), 5.05 (m, 1H), 3.74 (s, 3H), 1.63 (m, 1H), 1.47 (d, J=7.0 Hz, 3H), 0.65 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07462614B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-9c74f86ca13742c3bed036e945424a92 |
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| Source note | uspto-grants-2008_12 |
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