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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1442491Generated: October 31, 2026

Ethylamine hydrochloride → HCID 16222413, compound

https://huagongshe.com/reaction/1442491

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylamine hydrochlorideHCID 11198—
ReactantSodium BicarbonateHCID 516892—
ReactantMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
Reactant10H-Phenothiazine-2-carboxylic acidHCID 22711593—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 16222413HCID 16222413—

Reaction Conditions

Temperature0 °C

Reaction Steps

5.8 ml (3.3 eq.) of DIEAA is added dropwise to a solution of 2.43 g (10 mmoles) of 10H-phenothiazine-2-carboxylic acid, 1.79 g (2.2 eq.) of ethylamine hydrochloride and 4.17 g (1.1 eq.) of HBTU in 50 ml of DMF, cooled down to 0° C. The reaction mixture is stirred for 15 hours at 23° C., and then poured into a mixture of 100 ml of a saturated solution of NaHCO3 and 100 ml of AcOEt. After stirring for a few minutes, the precipitate formed is removed by filtration and the filtrate is decanted. The organic phase is successively washed with water, a 1M solution of citric acid and salt water. The organic solution is dried over sodium sulphate, filtered and concentrated to dryness under vacuum. The solid obtained is suspended in Et2O, triturated and filtered. A beige solid is obtained with a quantitative yield. Melting point: 150-151° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07659266B2
Source datasetuspto-grants-2010_02
ORD IDord-bd870c514088464da56ea09d83484b00
Source noteuspto-grants-2010_02