HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1409361Generated: November 3, 2026
Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) → HCID 66576287, compound
https://huagongshe.com/reaction/1409361
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 2733084 | — |
| Reactant | (S)-4-(1-(2-aminopropyl)-1H-pyrazol-3-yl)-2-chloro-6-fluorobenzonitrile | HCID 67170587 | — |
| Reactant | HCID 70980721 | HCID 70980721 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 66576287 | HCID 66576287 | 18.8% |
Reaction Steps
The title compound was prepared using the procedure described in Example 3(h) starting from 6-(methylsulfonamido)imidazo[1,2-a]pyridine-2-carboxylic acid (0.215 mmol, 0.055 g) and (S)-4-(1-(2-aminopropyl)-1H-pyrazol-3-yl)-2-chloro-6-fluorobenzo-nitrile (0.179 mmol, 0.050 g) using DCM (10 ml) as the solvent. HBTU (0.018 mmol, 6.80 mg) was used instead of HOBt. The mixture was diluted with DCM and washed with Na2CO3 solution and water. The organic phase was evaporated. The water phase and Na2CO3 phase were washed with EtOAc. The evaporated organic phases were combined and purified by preparative HPLC. 0.0174 g of the title compound was obtained. 1H-NMR (400 MHz, DMSO-d6): δ 1.14 (d, 3H), 3.04 (s, 3H), 4.27-4.58 (m, 3H), 7.00 (d, 1H), 7.27 (dd, 1H), 7.57-7.62 (m, 1H), 7.87 (d, 1H), 7.91 (dd, 1H), 7.95-7.97 (m, 1H), 8.36 (d, 1H), 8.49-8.51 (m, 1H), 8.55 (d, 1H), 9.77 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08921378B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-f6055661d0da49b7a4b3a1ee5632bdfd |
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| Source note | uspto-grants-2014_12 |
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