1-(2,4,5-trimethoxyphenyl)propan-2-amine [TMA-2]

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9 reactions in Reaxys

2016-06-19 14h:17m:05s (EST)

O NH 2

1. Query O O

Search as: As drawn

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O

O

O

O

O N

H 2N

O

O

O

Rx-ID: 297570 View in Reaxys 1/9 Yield

Conditions & References With hydrogenchloride, ethanol, acetic acid, Reduktion an Blei-Kathoden Bruckner; Journal fuer Praktische Chemie (Leipzig); vol. <2> 138; (1933); p. 268,270 View in Reaxys With lithium aluminium tetrahydride Bailey,K. et al.; Canadian Journal of Chemistry; vol. 49; (1971); p. 3143 - 3151 View in Reaxys Shulgin; Journal of medicinal chemistry; vol. 9; nb. 3; (1966); p. 445 - 446 View in Reaxys With lithium aluminium tetrahydride in tetrahydrofuran Ho,B.T. et al.; Journal of Medicinal Chemistry; vol. 13; (1970); p. 26 - 30 View in Reaxys (reduction) Shulgin,A.T.; Journal of Medicinal Chemistry; vol. 11; (1968); p. 186 - 187 View in Reaxys With lithium aluminium tetrahydride in diethyl ether Borchardt,R.T. et al.; Journal of Medicinal Chemistry; vol. 19; (1976); p. 1201 - 1209 View in Reaxys With lithium aluminium tetrahydride Zaitsu, Kei; Katagi, Munehiro; Kamata, Hiroe; Kamata, Tooru; Shima, Noriaki; Miki, Akihiro; Iwamura, Tatsunori; Tsuchihashi, Hitoshi; Journal of Mass Spectrometry; vol. 43; nb. 4; (2008); p. 528 - 534 View in Reaxys

O

O O

O

O

O

H 2N O

Rx-ID: 22646963 View in Reaxys 2/9 Yield

Conditions & References Reaction Steps: 2 1: NH4OAc 2: LiAlH4 / tetrahydrofuran With lithium aluminium tetrahydride, ammonium acetate in tetrahydrofuran Ho,B.T. et al.; Journal of Medicinal Chemistry; vol. 13; (1970); p. 26 - 30 View in Reaxys Reaction Steps: 2 1: NH4OAc / acetic acid 2: LiAlH4 / diethyl ether With lithium aluminium tetrahydride, ammonium acetate in diethyl ether, acetic acid Borchardt,R.T. et al.; Journal of Medicinal Chemistry; vol. 19; (1976); p. 1201 - 1209 View in Reaxys

Copyright © 2016 Reed Elsevier Properties SA. All rights reserved. Authorized use only. Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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O

O

O O H 2N O

O

Rx-ID: 22652419 View in Reaxys 3/9 Yield

Conditions & References Reaction Steps: 2 1: C(NO2)4, Py / acetone 2: LiAlH4 With pyridine, lithium aluminium tetrahydride, TNM in acetone Shulgin; Journal of medicinal chemistry; vol. 9; nb. 3; (1966); p. 445 - 446 View in Reaxys

O

O

H N H

O

HN

O

H

O

O

H

O

O

H 2N O

Rx-ID: 1378549 View in Reaxys 4/9 Yield

Conditions & References (i) H2, Pd-C, (ii) PhNCS, (iii) CF3CO2H, Multistep reaction Aldous,F.A.B. et al.; Journal of Medicinal Chemistry; vol. 17; (1974); p. 1100 - 1111 View in Reaxys

O

O

H N H

O

HN

O

H

O

O

H

O

O

H 2N O

Rx-ID: 1378550 View in Reaxys 5/9 Yield

Conditions & References (i) H2, Pd-C, (ii) PhNCS, (iii) CF3CO2H, Multistep reaction Aldous,F.A.B. et al.; Journal of Medicinal Chemistry; vol. 17; (1974); p. 1100 - 1111 View in Reaxys

O

O O

O H

H 2N O

H 2N O

Rx-ID: 22651071 View in Reaxys 6/9 Yield

Conditions & References Reaction Steps: 2 2: (i) H2, Pd-C, (ii) PhNCS, (iii) CF3CO2H Aldous,F.A.B. et al.; Journal of Medicinal Chemistry; vol. 17; (1974); p. 1100 - 1111

Copyright © 2016 Reed Elsevier Properties SA. All rights reserved. Authorized use only. Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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View in Reaxys

O

O O

O H

H 2N

H 2N

O

O

Rx-ID: 22651072 View in Reaxys 7/9 Yield

Conditions & References Reaction Steps: 2 2: (i) H2, Pd-C, (ii) PhNCS, (iii) CF3CO2H Aldous,F.A.B. et al.; Journal of Medicinal Chemistry; vol. 17; (1974); p. 1100 - 1111 View in Reaxys

O

O

O

O N

lead-cathodes

O

E

H 2N

O

O

O

Rx-ID: 7988901 View in Reaxys 8/9 Yield

Conditions & References Reduktion Bruckner; Journal fuer Praktische Chemie (Leipzig); vol. <2> 138; (1933); p. 268,270 View in Reaxys

O O

H 2N O

Rx-ID: 7297271 View in Reaxys 9/9 Yield

Conditions & References Oximinopropan (IV), H2 / Pd-C Patent; Merck and Co.; Inc.; BE633963; (1962); ; vol. 61; nb. 6953e; (1964) View in Reaxys Nitropropenyl-Verb., LiAlH4 Shulgin; Experientia; vol. 20; nb. 7; (1964); p. 366 - 367 View in Reaxys

Copyright © 2016 Reed Elsevier Properties SA. All rights reserved. Authorized use only. Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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