Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantN,N-Dimethylglycine hydrochlorideHCID 75605—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant3-Amino-5-(3,5-dimethylisoxazol-4-yl)-3-phenylindolin-2-oneHCID 86280821—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product2-(Dimethylamino)-N-(5-(3,5-dimethylisoxazol-4-yl)-2-oxo-3-phenylindolin-3-yl)acetamideHCID 8628190340%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09393232B2
Source datasetuspto-grants-2016_07
ORD IDord-e542b75dbdae4212a27555eadc5d9f56
Source noteuspto-grants-2016_07