HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1874767Generated: November 1, 2026
Diisopropylethylamine → N-({4-chloro-3-[(3-chloro-5-cyanophenyl)oxy]phenyl}methyl)-6-(methyloxy)-1H-indole-3-carboxamide
https://huagongshe.com/reaction/1874767
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 | 6-Methoxy-1H-indole-3-carboxylic acid | HCID 17750956 | — |
| Reactant | 3-{[5-(Aminomethyl)-2-chlorophenyl]oxy}-5-chlorobenzonitrile | HCID 59451405 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | N-({4-chloro-3-[(3-chloro-5-cyanophenyl)oxy]phenyl}methyl)-6-(methyloxy)-1H-indole-3-carboxamide | HCID 59451549 | 75.7% |
Reaction Steps
N-({4-Chloro-3-[(3-chloro-5-cyanophenyl)oxy]phenyl}methyl)-6-(methyloxy)-1H-indole-3-carboxamide was prepared in a similar manner as described herein from 3-{[5-(aminomethyl)-2-chlorophenyl]oxy}-5-chlorobenzonitrile (0.05 g, 0.17 mmol), 6-(methyloxy)-1H-indole-3-carboxylic acid, (0.035 g, 0.18 mmol), HATU (0.1 g, 0.25 mmol), DIPEA (0.05 mL, 0.25 mmol), acetonitrile (3 mL) and DMF (1 mL). The crude material was purified by Reverse-Phase HPLC (water/acetonitrile with 0.1% TFA). The desired fractions were neutralized and extracted with EtOAc. The organic extracts were combined, dried over Na2SO4, filtered and evaporated to afford the title compound (0.06 g, 75%) as a white solid. 1H NMR (400 MHz, DMSO-d6): δ ppm 11.33 (br. s., 1H), 8.39 (s, 1H), 7.93 (d, 1H), 7.86 (d, 1H), 7.77 (d, 1H), 7.58 (d, 1H), 7.43 (dd, 1H), 7.34 (t, 1H), 7.27 (dd, 1H), 7.22 (d, 1H), 6.88 (d, 1H), 6.71 (dd, 1H), 4.43 (d, 2H), 3.74 (s, 3H). MS: m/z 466.0 (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-ee8bf5f7521f4a1996df59be3906af95 |
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| Source note | uspto-grants-2012_11 |
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