HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1413002Generated: November 1, 2026
Diisopropylethylamine → HCID 178495706, compound
https://huagongshe.com/reaction/1413002
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | (2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoic acid | HCID 59540170 | — |
| Reactant | HCID 178495689 | HCID 178495689 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178495706 | HCID 178495706 | — |
Reaction Steps
A mixture of tert-butyl(2S,4S)-4-(methoxymethyl)-2-(5-{2-[(2S,5S)-5-methylpyrrolidin-2-yl]-1,11-dihydroisochromeno[4′,3′:6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)pyrrolidine-1-carboxylate (101 mg, 0.159 mmol), (2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoic acid (30 mg, 0.159 mmol), HATU (61 mg, 0.159 mmol) and 2 mL 10% DIPEA in DMF was stirred at room temperature for 1.5 hours. Saturated sodium bicarbonate was added and the product was extracted into dichloromethane, dried over sodium sulphate, filtered and concentrated under reduced pressure. This crude product was treated with 5 mL 1.25N HCl in ethanol at 50° C. for 4 h and then it was concentrated under reduced pressure. Saturated sodium bicarbonate was added and the product was extracted into dichloromethane, dried over sodium sulphate, filtered and concentrated under reduced pressure. (74.6 mg)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08921341B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-257ae11e8e224a97af72e338b441c329 |
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| Source note | uspto-grants-2014_12 |
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