HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1815925Generated: November 1, 2026
Diisopropylethylamine → HCID 10223056, compound
https://huagongshe.com/reaction/1815925
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | N-(3-Aminophenyl)acrylamide | HCID 22033841 | — |
| Reactant | HCID 22496109 | HCID 22496109 | — |
| Product | HCID 10223056 | HCID 10223056 | — |
Reaction Steps
To a slurry of 7-chloro-1-(4-chloro-[1,3,5]triazin-2-yl)-1,2,3,4-tetrahydro-quinoline (Step 2)(70 mg, 0.249 mmol) in IpOH (2.0 ml) was added DIEA (0.20 mL, 1.15 mmol) and N-(3-aminophenyl)acrylamide (100 mg, 0.192 mmol). The heated at 100° C. for 18 h, then cooled to RT. The organics were concentrated under reduced pressure then purified by column chromatography (elution with CH2Cl2 followed by 99:1 CH2Cl2/MeOH followed by 97:3 CH2Cl2/MeOH) to give N-{3-[4-(7-chloro-3,4-dihydro-2H-quinolin-1-yl)-[1,3,5]triazin-2-ylamino]-phenyl}-acrylamide: MS m/z=407 [M+H]+. Calc'd for C21H19ClN6O: 406.13.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06881737B2 |
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| Source dataset | uspto-grants-2005_04 |
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| ORD ID | ord-c4386dd81e464d48add07cdb21533274 |
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| Source note | uspto-grants-2005_04 |
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