HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2205300Generated: October 31, 2026
Triethylamine → 4'-(Cyclopropylcarbamoyl)biphenyl-4-yl N-methyl-N-(3-(pyridin-4-yl)benzyl)carbamate
https://huagongshe.com/reaction/2205300
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-methyl(3-(pyridin-4-yl)phenyl)methanamine | HCID 7060574 | — |
| Reactant | 4-[4-(Cyclopropylcarbamoyl)phenyl]phenyl 2,5-dioxopyrrolidin-1-yl carbonate | HCID 86722072 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4'-(Cyclopropylcarbamoyl)biphenyl-4-yl N-methyl-N-(3-(pyridin-4-yl)benzyl)carbamate | HCID 71492972 | — |
Reaction Steps
Into a 100-mL round-bottom flask was placed a solution of 4-[4-(cyclopropylcarbamoyl)phenyl]phenyl 2,5-dioxopyrrolidin-1-yl carbonate (600 mg, 1.52 mmol, 1.00 equiv) in dichloromethane (40 mL), N-methyl([[3-(pyridin-4-yl)phenyl]methyl])amine (301 mg, 1.52 mmol, 1.00 equiv) and triethylamine (153 mg, 1.51 mmol, 0.99 equiv). The resulting solution was stirred overnight at room temperature. The reaction mixture was washed with 2×20 mL of water and dried over anhydrous sodium sulfate. The resulting mixture was concentrated under vacuum. The crude product (650 mg) was purified by Prep-HPLC with the following conditions (1#-Pre-HPLC-002(Agilent)): Column, SunFire Prep C18, 19*150 mm 5 um; mobile phase, water and acetonitrile (10.0% acetonitrile up to 80.0% in 10 min, up to 100.0% in 1 min, down to 10.0% in 2 min); Detector, uv 220 & 254 nm. The title compound was obtained as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09371285B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-80ae7334799b4a40a0485554ca6c3d1e |
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| Source note | uspto-grants-2016_06 |
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