HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1176051Generated: November 4, 2026
Diisopropylethylamine → HCID 178507987, compound
https://huagongshe.com/reaction/1176051
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 6-Amino-3-oxo-2,3-dihydro-indazole-1-carboxylic acid tert-butyl ester | HCID 57498019 | — |
| Reactant | HCID 178526743 | HCID 178526743 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178507987 | HCID 178507987 | 33.6% |
Reaction Steps
To a solution of (6-chloro-5-nitro-pyrimidin-4-yl)-(5-cyclopropyl-2H-pyrazol-3-yl)-amine (50 mg, 0.18 mmol) in anhydrous THF (2 mL) was added 6-amino-3-oxo-2,3-dihydro-indazole-1-carboxylic acid tert-butyl ester (67 mg, 0.27 mmol) and diisopropylethylamine (23 mg, 0.18 mmol). The mixture was stirred at RT for 14 hrs and the solvents were removed under vacuum. The residue was dissolved in CH2Cl2 (3 mL) and treated with TFA (2 mL) at RT for 2 hrs. After removal of the solvents via evaporation, the residue was reduced by hydrogen (50 psi) in MeOH (10 mL) in the presence of Pd/C (10%, 50 mg) for 3 hrs. The solution was filtered via celite, the filtrate was evaporated under vacuum, and the residue was purified by HPLC to give the desired product as white solid (22 mg). NMR (500 MHz, DMSO-d6) δ11.16 (br, 1H), 9.92 (br, 1H), 8.98 (s, 1H), 8.27 (s, 1H), 7.67 (s, 1H), 7.55 (d, 1H), 7.08 (d, 1H), 5.95 (s, 1H), 2.00 (m, 1H), 1.06 (m, 2H), 0.81 (m, 2H) ppm. MS (ES+): m/e=364.3 (M+H); LC/Method A/2.45 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07842712B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-8e7db69e501d477b8810a3b9318965cb |
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| Source note | uspto-grants-2010_11 |
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