HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1052986Generated: October 30, 2026
Triethylamine → 2-(Dimethylamino)-N-(5-(3,5-dimethylisoxazol-4-yl)-2-oxo-3-phenylindolin-3-yl)acetamide
https://huagongshe.com/reaction/1052986
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N,N-Dimethylglycine hydrochloride | HCID 75605 | — |
| 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-Amino-5-(3,5-dimethylisoxazol-4-yl)-3-phenylindolin-2-one | HCID 86280821 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(Dimethylamino)-N-(5-(3,5-dimethylisoxazol-4-yl)-2-oxo-3-phenylindolin-3-yl)acetamide | HCID 86281903 | 40% |
Reaction Steps
A mixture of 2-(dimethylamino)acetic acid hydrochloride (87 mg, 0.62 mmol), HATU (118 mg, 0.31 mmol), and Et3N (94 mg, 0.93 mmol) in CH2Cl2 (10 mL) was stirred at RT for 0.5 hours, and then 3-amino-5-(3,5-dimethylisoxazol-4-yl)-3-phenylindolin-2-one (100 mg, 0.31 mmol) was added and the mixture was stirred for another 12 h. And water (10 mL) was added, the mixture was extracted with CH2Cl2 (2×20 mL), combined organic phase, washed with brine (20 mL), dried with Na2SO4, concerned in vacuo, the mixture was purified with column chromatography to give product (50 mg, 40%) as a solid. 1H NMR (400 MHz, DMSO-d6): δH 10.70 (s, 1H), 9.74 (s, 1H), 7.26-7.40 (m, 7H), 6.99 (d, J=8.0 Hz, 1H), 4.07 (d, J=16.0 Hz, 1H), 3.93 (d, J=16.0 Hz, 1H), 2.78 (s, 3H), 2.71 (s, 3H), 2.38 (s, 3H), 2.20 (s, 3H). MS (ESI) m/e [M+1]+ 405.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09393232B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-e542b75dbdae4212a27555eadc5d9f56 |
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| Source note | uspto-grants-2016_07 |
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