HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 331082Generated: October 30, 2026
Diisopropylethylamine → HCID 59333961, compound
https://huagongshe.com/reaction/331082
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Triphosgene | HCID 94429 | — |
| Reactant | HCID 68595581 | HCID 68595581 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59333961 | HCID 59333961 | — |
Reaction Steps
To a −78° C. solution of N-(4-ethoxypyrimidin-2-yl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-amine hydrochloride (0.300 g, 1.09 mmol) in CH2Cl2 (15 mL) and diisopropylethylamine (0.952 mL, 5.47 mmol) was added triphosgene (0.227 g, 0.766 mmol) in CH2Cl2 (5 mL) dropwise over 10 min. The reaction was quenched with H2O (10 mL), warmed to 22° C., and made pH 8-9 with NaHCO3. The aqueous layer was extracted with CH2Cl2 (2×30 mL) and the combined organic layers washed with brine (1×30 mL), dried over MgSO4, and concentrated to give the desired product M1(i) as a brown solid (0.35 g, 95%). Mass Spectrum: Calcd for C14H18ClN6O2 (M+H): 337. Found: 337.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08877761B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-167b2c32fc264364a31189a8859c1369 |
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| Source note | uspto-grants-2014_11 |
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