HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 331078Generated: October 30, 2026
Diisopropylethylamine → HCID 59333959, compound
https://huagongshe.com/reaction/331078
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Fluoro-1-methyl-4-piperidinecarbonyl chloride | HCID 21050390 | — |
| Reactant | HCID 68595875 | HCID 68595875 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59333959 | HCID 59333959 | — |
Reaction Steps
To a solution of ethyl 3-[(2-ethoxy-5-fluoropyrimidin-4-yl)amino]-6,6-dimethyl-5,6-dihydropyrrolo[3,4-c]pyrazole-1(4H)-carboxylate dihydrochloride (120 mg, 0.27 mmol) in 15 mL THF containing diisopropylethyl amine (0.23 mL, 4 eq) was added a 5 mL THF suspension of 4-fluoro-1-methylpiperidine-4-carbonyl chloride (128 mg, 2.6 eq). After heating for 5 hours at 65° C., the reaction was concentrated to dryness and carried on without further purification. To a solution of ethyl 3-[(2-ethoxy-5-fluoropyrimidin-4-yl)amino]-5-[(4-fluoro-1-methylpiperidin-4-yl)carbonyl]-6,6-dimethyl-5,6-dihydropyrrolo[3,4-c]pyrazole-1(4H)-carboxylate in methanol was added 2 mL of a 10% sodium hydroxide solution in methanol. After removing the solvent in vacuo, the residue was purified as in Example K1 above. See Table 1 below for NMR data.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08877761B2 |
|---|
| Source dataset | uspto-grants-2014_11 |
|---|
| ORD ID | ord-8cfbbd3c40a3480c9699f8f094bfd9ef |
|---|
| Source note | uspto-grants-2014_11 |
|---|