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[ CAS No. 121821-01-0 ] {[proInfo.proName]}

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Chemical Structure| 121821-01-0
Chemical Structure| 121821-01-0
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Product Details of [ 121821-01-0 ]

CAS No. :121821-01-0 MDL No. :MFCD00035196
Formula : C11H13ClN2O2 Boiling Point : -
Linear Structure Formula :- InChI Key :GEFZFHTWRMQGOO-UHFFFAOYSA-N
M.W : 240.69 Pubchem ID :14374493
Synonyms :

Safety of [ 121821-01-0 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P305+P351+P338 UN#:N/A
Hazard Statements:H319 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 121821-01-0 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 121821-01-0 ]

[ 121821-01-0 ] Synthesis Path-Downstream   1~13

  • 1
  • [ 121821-01-0 ]
  • [ 22641-00-5 ]
YieldReaction ConditionsOperation in experiment
With triethylamine In toluene at 70℃;
  • 2
  • [ 121821-01-0 ]
  • [ 98-59-9 ]
  • [ 38353-77-4 ]
YieldReaction ConditionsOperation in experiment
98% With pyridine; triethylamine for 4h; Ambient temperature;
  • 3
  • [ 22641-00-5 ]
  • [ 121821-01-0 ]
YieldReaction ConditionsOperation in experiment
98% With hydrogenchloride In ethanol at 75℃; for 5h;
  • 4
  • [ 121821-01-0 ]
  • [ 199522-67-3 ]
  • 1-{2-[(5-bromo-pyridin-2-yl)-(3,4-dichloro-benzyl)-amino]-ethyl}-3-[3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-propyl]-thiourea [ No CAS ]
YieldReaction ConditionsOperation in experiment
85% With triethylamine In tetrahydrofuran Ambient temperature;
  • 5
  • [ 10513-96-9 ]
  • [ 121821-01-0 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: N2H4*H2O / ethanol; dimethylformamide 2: 98 percent / 2M HCl / ethanol / 5 h / 75 °C
  • 6
  • [ 121821-01-0 ]
  • [ 56642-94-5 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 4 steps 1: 98 percent / Et3N, pyridine / 4 h / Ambient temperature 2: NaNO2 / acetic acid; acetic anhydride / 3 h / 5 °C 3: benzene / 20 h / 80 °C 4: 95 percent / Cs2CO3 / dimethylformamide / 48 h / Ambient temperature
Multi-step reaction with 2 steps 1: 98 percent / Et3N, pyridine / 4 h / Ambient temperature 2: 95 percent / Cs2CO3 / dimethylformamide / 48 h / Ambient temperature
  • 7
  • [ 121821-01-0 ]
  • [ 88597-06-2 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1: 98 percent / Et3N, pyridine / 4 h / Ambient temperature 2: NaNO2 / acetic acid; acetic anhydride / 3 h / 5 °C 3: benzene / 20 h / 80 °C
  • 8
  • [ 121821-01-0 ]
  • [ 88597-05-1 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: 98 percent / Et3N, pyridine / 4 h / Ambient temperature 2: NaNO2 / acetic acid; acetic anhydride / 3 h / 5 °C
  • 9
  • [ 121821-01-0 ]
  • [ 107976-61-4 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 4 steps 1: 98 percent / Et3N, pyridine / 4 h / Ambient temperature 2: NaNO2 / acetic acid; acetic anhydride / 3 h / 5 °C 3: benzene / 20 h / 80 °C 4: 99 percent / Cs2CO3 / dimethylformamide / 48 h / Ambient temperature
  • 10
  • [ 121821-01-0 ]
  • [ 121821-26-9 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 4 steps 1: 98 percent / Et3N, pyridine / 4 h / Ambient temperature 2: NaNO2 / acetic acid; acetic anhydride / 3 h / 5 °C 3: benzene / 20 h / 80 °C 4: 88 percent / Cs2CO3 / dimethylformamide / 48 h / Ambient temperature
  • 11
  • [ 121821-01-0 ]
  • [ 121821-31-6 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 4 steps 1: 98 percent / Et3N, pyridine / 4 h / Ambient temperature 2: NaNO2 / acetic acid; acetic anhydride / 3 h / 5 °C 3: benzene / 20 h / 80 °C 4: 98 percent / Cs2CO3 / dimethylformamide / 48 h / Ambient temperature
  • 12
  • [ 121821-01-0 ]
  • [ 121821-32-7 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 4 steps 1: 98 percent / Et3N, pyridine / 4 h / Ambient temperature 2: NaNO2 / acetic acid; acetic anhydride / 3 h / 5 °C 3: benzene / 20 h / 80 °C 4: 99 percent / Cs2CO3 / dimethylformamide / 48 h / Ambient temperature
  • 13
  • [ 141-82-2 ]
  • [ 121821-01-0 ]
  • C14H14N2O5 [ No CAS ]
YieldReaction ConditionsOperation in experiment
11% With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate In N,N-dimethyl-formamide at 23℃; for 3h; C To a solution of 2-(3-aminopropyl)isoindoline-l,3-dione hydrochloride (49.8 mg, 0.207 mmol), malonic acid (43.1 mg, 2.0 equiv.), and DIPEA (0.11 mL, 3.0 equiv.) in DMF (0.9 mL) was added HATU (157.3 mg, 2.0 equiv.). The reaction mixture was agitated at ambient temperature for 3 hours and then purified by preparative HPLC (H20/MeCN with 0.1% TFA) to afford 6.7 mg (11% yield) of 1-94 as a colorless oil. ESI-MS: Found 291.1, C14H15N2O5 (MH+) requires 291.1
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