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Chemical Structure| 49844-36-2 Chemical Structure| 49844-36-2

Structure of 49844-36-2

Chemical Structure| 49844-36-2

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Product Details of [ 49844-36-2 ]

CAS No. :49844-36-2
Formula : C15H16ClNO2
M.W : 277.75
SMILES Code : O=C(C1C(NC2=C3C=C(Cl)C=C2)=C3CCC1)OCC
MDL No. :MFCD02766766

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Application In Synthesis of [ 49844-36-2 ]

* 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 [ 49844-36-2 ]

[ 49844-36-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 49844-36-2 ]
  • [ 49843-98-3 ]
YieldReaction ConditionsOperation in experiment
78% With ammonia; In ethanol; at 60 - 75℃; for 24.75h; 2 (10 g, 40 mmole) was dissolved in ethanol (100 mL) 7M ammonia in ethanol (200 mL) was added and the material transferred to a Parr pressure reactor. The reaction vessel was purged briefly to displace any air with ammonia vapor. The reaction was then heated to 60 C. The reaction temperature overshot to 75 C. briefly then returned to 60 C. within 45 min. The material was stirred at this temperature for 24 hours. The reaction was then cooled to room temperature and the solvent removed in vacuo. This gave the crude product (9.6 gms) as an off-white foam. The material was chromatographed twice on a Biotage 40L column. The first chromatography, elution with 100% ethyl acetate, failed to remove a trace impurity. A second chromatography utilizing a step gradient (starting with 1/1 heptane/ethyl acetate jumping to 1/4 heptane/ethyl acetate as the impurity began to elute) provided clean 4 (7.8 g, 31.4 mmole, 78%) as an off-white crystalline solid. (7.8 g, 31.4 mmole, 78%) as an off-white crystalline solid. 1H NMR delta (CD3OD, ppm) 7.34-7.38 (s, 1H), 7.20-7.24 (m, 1H), 6.95-7.03 (m, 1H), 3.69-3.75 (m, 1H), 2.59-2.75 (m, 2H), 1.76-2.20 (m, 4H).
45% With ammonia; In methanol; at 100℃; under 7600.51 Torr; for 15.0h; Step 3: Ethyl 6-chloro-2,3,4,9-tetrahydro-1H-carbazole-1-carboxylate (1 g, 3.60 mmol, 1.00 equiv) (step 2) and NH3 (7M in MeOH) (15 mL) were added into a 30 mL pressure tank reactor (10 atm). The resulting solution was stirred for 15 h at 100 C. The resulting mixture was concentrated under vacuum. The crude product was purified by Prep-HPLC with the following conditions: Column,)(Bridge Shield RP18 OBD Column, 5 mum, 19*150 mm; mobile phase, water (0.05% TFA) and ACN (31.0% ACN up to 42.0% in 10 min); Detector, UV 254/220 nm. This resulted in 400 mg (45%) of 6-chloro-2,3,4,9-tetrahydro-1H-carbazole-1-carboxamide as a white solid. 1H NMR (400 MHz, DMSO-d6) delta: 10.81 (s, 1H), 7.44-7.36 (m, 2H), 7.29 (m, 1H), 7.10 (s, 1H), 7.00 (m, 1H), 3.66 (m, 1H), 2.64-2.56 (m, 2H), 2.11-1.89 (m, 3H), 1.70 (m, 1H). LC-MS: m/z=249 [M+H]+.
88.3 kg With ammonia; In methanol; at 0 - 50℃; under 3000.3 Torr; for 51.0h;Large scale; Example 6: stage 3 procedure using pure ammoniaA solution of 6-chloro-2,3,4,9-tetrahydro-lH-carbazole-l-carboxylic acid ethyl ester (183 kg) in MeOH (850 1) in a pressure reactor was cooled to 5±5C, and ammonia (328 kg) was added over 4 h while stirring at to 5±5C. Then the temperature was increased to 45±5C (4 bar internal pressure) and kept at this temperature for 47 h (HPLC check: no s.m. left).The solution was cooled to 0 - 10C, filtered into a non-pressure reactor and warmed to 45±5C over 4 h and kept at this temperature for another 12 h to gas off the excess ammonia. After charcoal treatment (8 kg) at 60C, filtration, washing with MeOH (150 1) and evaporation of solvent (300 1), water (200 1) is added and the mixture is cooled to 3±3C to precipitate 6-chloro-2,3,4,9-tetrahydro-lH-carbazole-l -carboxylic acid amide product. The solid is centrifuged and drummed off for the subsequent recrystallisation. Yield: 142 kg. With a LOD = 16% this corresponds to 1 19 kg dry material (81.3% of theory).This material, dissolved in in methyethyl ketone (407 kg) is heated to reflux, and cyclohexane is added at to 68 -77C over 15 min. The mixture is stirred at to 68C for 1.5h, then it is cooled to 0C over 2h. The solid is isolated by centrifugation (146 kg, wet).The solid is suspended in 2-propanol heated to reflux within 2h 20 min(complete dissolution), then cooled to 0±5C over 2.5h and kept at to 0±5C for lh. The solid is centrifuged and then dried for 18 in a paddle dryer (to 20 - 49C, 28 - 86 mbar) to give the final product (88.3 kg).
 

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