HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 7087Generated: October 29, 2026
Diisopropylethylamine → HCID 178418888, compound
https://huagongshe.com/reaction/7087
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | [2-(chloromethyl)-1H-benzimidazol-5-yl](phenyl)methanone | HCID 1951252 | — |
| Reactant | N-(t-butoxycarbonyl)-N-(2-pyridinylmethyl)-N'-(5,6,7,8-tetrahydro-8-quinolinyl)-1,4-benzenedimethanamine | HCID 22018600 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178418888 | HCID 178418888 | 75.9% |
Reaction Steps
A solution of 5-benzoyl-2-chloromethylbenzimidazole (284 mg, 1.05 mmol), N-(tert-butoxycarbonyl)-N-(2-pyridinylmethyl)-N′-(5,6,7,8-tetrahydro-8-quinolinyl)-1,4-benzenedimethanamine (476 mg, 1.04 mmol) and N,N-diisopropylethylamine (0.36 mL, 2.08 mmol) were stirred at 80□ C in DMF (4 mL) for 16 hours. The reaction was then cooled, concentrated under reduced pressure and diluted with CH2Cl2 (35 mL) and saturated aqueous NaHCO3 (40 mL). The phases were separated and the aqueous phase was washed with CH2Cl2 (2×25 mL). The combined organic extracts were washed with saturated aqueous NaHCO3 (1×40 mL), dried (NaSO4), filtered and concentrated under reduced pressure. Purification of the resultant oil by flash chromatography on silica gel (96:4 CH2Cl2/MeOH) provided the desired alkylated product (468 mg, 65%) as an orange oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07084155B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-c3e65d3523c4435f91103dac99cfb3aa |
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| Source note | uspto-grants-2006_08 |
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