HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1795885Generated: October 26, 2026
Diisopropylethylamine → HCID 178427890, compound
https://huagongshe.com/reaction/1795885
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | PyBOP | HCID 2724699 | — |
| Reactant | O-(cyclopropylmethyl)hydroxylamine hydrochloride | HCID 11557279 | — |
| Reactant | HCID 178427892 | HCID 178427892 | — |
| Solvent | Tetrahydrofurane dichloromethane | HCID 21919333 | — |
| Product | HCID 178427890 | HCID 178427890 | — |
Reaction Steps
A solution comprised of 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-1H-benzoimidazole-5-carboxylic acid, O-cyclopropylmethylhydroxylamine hydrochloride (1.25 equiv.), benzotriazole-1-yl-oxy-tris-pyrrolidino-phosphonium hexafluorophosphate (1.25 equiv.), and diisopropylethylamine (3 equiv.) in 1:1 v/v tetrahydrofuran-dichloromethane is stirred for 30 minutes. The reaction mixture is concentrated in vacuo and the residue is taken up into diethyl ether. The ether phase is washed with dilute aqueous hydrochloric acid, saturated aqueous sodium bicarbonate, and brine, is dried (MgSO4), and is concentrated in vacuo to afford the desired product. The product may be recrystallized with an appropriate solvent like methanol or chloroform if further purification is necessary.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07030119B1 |
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| Source dataset | uspto-grants-2006_04 |
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| ORD ID | ord-e02dbbd0a385419dbb78fce771597d84 |
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| Source note | uspto-grants-2006_04 |
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