N,1-二甲基色胺

N,1-二甲基色胺
英文名	N,1-Dimethyltryptamine
別名	N,N'-二甲基色胺
識別
CAS號	37637-29-9
性質
化學式	C12H16N2
摩爾質量	188.27 g·mol−1
溶解性（水）	可溶於水（1.8 g，25 °C），易溶於酸
	若非註明，所有數據均出自標準狀態（25 ℃，100 kPa）下。

N,1-二甲基色胺是一種有機化合物，化學式為C₁₂H₁₆N₂，它是二甲基色胺的同分異構體之一，為芳環氮和氨基氮上的氫各被一個甲基取代的產物。它可由N-叔丁氧羰基-N,1-二甲基色胺在三氟乙酸的二氯甲烷溶液中脫Boc保護得到^[2]，或由相應的酰胺還原得到^[3]。它的氨基氮上可以進一步甲基化，得到季銨鹽^[2]。

參考文獻

^ Calculated using Advanced Chemistry Development (ACD/Labs) Software V11.02 (© 1994-2021 ACD/Labs). Retrieved from SciFinder. [2021-07-22].
^ ^2.0 ^2.1 Pérez, Edwin G.; Cassels, Bruce K.; Eibl, Christoph; Gündisch, Daniela. Synthesis and evaluation of N1-alkylindole-3-ylalkylammonium compounds as nicotinic acetylcholine receptor ligands. Bioorganic & Medicinal Chemistry. 2012-06, 20 (12): 3719–3727. doi:10.1016/j.bmc.2012.04.050 （英語）.
^ Jamison, Christopher R.; Badillo, Joseph J.; Lipshultz, Jeffrey M.; Comito, Robert J.; MacMillan, David W. C. Catalyst-controlled oligomerization for the collective synthesis of polypyrroloindoline natural products. Nature Chemistry. 2017-12, 9 (12): 1165–1169 [2022-03-23]. ISSN 1755-4330. doi:10.1038/nchem.2825. （原始內容存檔於2022-03-13）（英語）.

[1] Calculated using Advanced Chemistry Development (ACD/Labs) Software V11.02 (© 1994-2021 ACD/Labs). Retrieved from SciFinder. [2021-07-22].

[Perez-2] 2.0 ^2.1 Pérez, Edwin G.; Cassels, Bruce K.; Eibl, Christoph; Gündisch, Daniela. Synthesis and evaluation of N1-alkylindole-3-ylalkylammonium compounds as nicotinic acetylcholine receptor ligands. Bioorganic & Medicinal Chemistry. 2012-06, 20 (12): 3719–3727. doi:10.1016/j.bmc.2012.04.050 （英語）.

[3] Jamison, Christopher R.; Badillo, Joseph J.; Lipshultz, Jeffrey M.; Comito, Robert J.; MacMillan, David W. C. Catalyst-controlled oligomerization for the collective synthesis of polypyrroloindoline natural products. Nature Chemistry. 2017-12, 9 (12): 1165–1169 [2022-03-23]. ISSN 1755-4330. doi:10.1038/nchem.2825. （原始內容存檔於2022-03-13）（英語）.

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