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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264596Generated: October 31, 2026

Triethylamine → 5-(6-Amino-pyrimidin-4-yloxy)-2,3-dihydro-indole-1-carboxylic acid [3-(4-isopropylpiperazin-1-ylmethyl)-5-trifluoromethyl-phenyl]-amide

https://huagongshe.com/reaction/2264596

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTriphosgeneHCID 94429—
Reactant3-(4-Isopropylpiperazin-1-ylmethyl)-5-trifluoromethyl-anilineHCID 57431442—
Reactant5-(6-amino-pyrimidin-4-yloxy)-2,3-dihydro-1H-indoleHCID 67530482—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
SolventSodium CarbonateHCID 10340—
Product5-(6-Amino-pyrimidin-4-yloxy)-2,3-dihydro-indole-1-carboxylic acid [3-(4-isopropylpiperazin-1-ylmethyl)-5-trifluoromethyl-phenyl]-amideHCID 59596408—

Reaction Steps

49 mg (0.16 mMol) triphosgene are dissolved in 5 ml ice-cooled CH2Cl2. Then a solution of 149 mg (0.49 mMol) 5-trifluoromethyl-3-(4-isopropylpiperazin-1-ylmethyl)-aniline and 98 μl (0.70 mMol) Et3N in 2 ml CH2Cl2 is added during 5 min. After 3 additional minutes, the mixture is warmed up to rt by a water bath and then a solution of 0.47 mMol 5-(6-amino-pyrimidin-4-yloxy)-2,3-dihydro-1H-indole (Step 20.3) and 65 μl (0.47 mMol) Et3N in 2 ml CH2Cl2 is added during 5 min. After 2 h at rt, the mixture is diluted with sat. Na2CO3 solution/water 1:1 and EtOAc, the aqueous phase separated off and extracted twice with EtOAc. The organic layers are washed with water and brine, dried (Na2SO4) and concentrated. Reversed phase MPLC (Gilson system) gives the title compound: MS: [M+1]+=556; HPLC: AtRet=9.7.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855215B2
Source datasetuspto-grants-2010_12
ORD IDord-45e9f3aa833040bf9cb2ccdcb884fb62
Source noteuspto-grants-2010_12