HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1875049Generated: October 30, 2026
Diisopropylethylamine → 3-chloro-N-{[4-chloro-2-fluoro-3-(1-naphthalenyloxy)phenyl]methyl}-1H-pyrrole-2-carboxamide
https://huagongshe.com/reaction/1875049
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| 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 | 3-chloro-1H-pyrrole-2-carboxylic acid | HCID 22180018 | — |
| Reactant | {[4-Chloro-2-fluoro-3-(1-naphthalenyloxy)phenyl]methyl}amine | HCID 68486009 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-chloro-N-{[4-chloro-2-fluoro-3-(1-naphthalenyloxy)phenyl]methyl}-1H-pyrrole-2-carboxamide | HCID 59451634 | 21.1% |
Reaction Steps
HATU (0.113 g, 0.298 mmol) was added to a solution of {[4-chloro-2-fluoro-3-(1-naphthalenyloxy)phenyl]methyl}amine (0.060 g, 0.199 mmol) and 3-chloro-1H-pyrrole-2-carboxylic acid (0.0289 g, 0.199 mmol) nd diisopropylethylamine (0.052 mL, 0.298 mmol) and diisopropylethylamine (0.052 mL, 0.298 mmol) in DMF (1 mL). The mixture was stirred at room temperature for 1 hr. The reaction mixture was extracted with ethyl acetate and water. The organic layer was washed with water and brine, dried over sodium sulfate and concentrated. The residue was purified by reverse phase HPLC (acetonitrile:water with 0.1% TFA) to give the title compound (0.018 g, 21%) as a white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 11.80 (br. s., 1H), 8.29-8.40 (m, 1H), 7.91-8.04 (m, 2H), 7.57-7.69 (m, 3H), 7.51 (dd, 1H), 7.35 (t, 2H), 6.93 (t, 1H), 6.52 (d, 1H), 6.19 (t, 1H), 4.54 (d, 2H). ES MS: m/z 429 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08304419B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-3fc46b1568a3414da1be54b197bb57e0 |
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| Source note | uspto-grants-2012_11 |
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