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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Triphosgene | HCID 94429 | — |
| Reactant | 3-(4-Isopropylpiperazin-1-ylmethyl)-5-trifluoromethyl-aniline | HCID 57431442 | — |
| Reactant | 5-(6-amino-pyrimidin-4-yloxy)-2,3-dihydro-1H-indole | HCID 67530482 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Sodium Carbonate | HCID 10340 | — |
| Product | 5-(6-Amino-pyrimidin-4-yloxy)-2,3-dihydro-indole-1-carboxylic acid [3-(4-isopropylpiperazin-1-ylmethyl)-5-trifluoromethyl-phenyl]-amide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07855215B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-45e9f3aa833040bf9cb2ccdcb884fb62 |
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| Source note | uspto-grants-2010_12 |
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