HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2041750Generated: November 2, 2026
HCID 68184860, compound → HCID 68161437, compound
https://huagongshe.com/reaction/2041750
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 68184860 | HCID 68184860 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 68161437 | HCID 68161437 | 91% |
Reaction Steps
A solution of 1,1-dimethylethyl (2-{4-[(2S,4R)-1-acetyl-2-methyl-4-(3-pyridinylamino)-1,2,3,4-tetrahydro-6-quinolinyl]-1H-pyrazol-1-yl}ethyl)methylcarbamate (for a preparation see intermediate 58) (84 mg, 0.166 mmol) in dichloromethane (DCM) (3 mL) at room temperature under nitrogen was treated with trifluoroacteic acid TFA (0.5 mL, 6.49 mmol) and the resulting mixture was stirred at this temperature for 1 h then concentrated in vacuo. The residue was loaded onto a 10 G SCX cartridge and eluted with MeOH (2×20 mL) then with a 2N NH3 in MeOH (20 mL). The ammonia fractions were collected and concentrated in vacuo to give (2S,4R)-1-acetyl-2-methyl-6-{1-[2-(methylamino)ethyl]-1H-pyrazol-4-yl}-N-3-pyridinyl-1,2,3,4-tetrahydro-4-quinolinamine (61 mg, 0.151 mmol, 91%) as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08580957B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-2f3ed72a52ad496cb50b09ae40c6c433 |
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| Source note | uspto-grants-2013_11 |
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