CAS
214603-97-1 Purity
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214603-97-1 Purity
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tert-Butyl 2-oxo-2,3-dihydroindole-1-carboxylate
CAS
214610-10-3
Catalog Number
ACM214610103
Category
Other Products
Molecular Weight
233.263100 [g/mol]
Molecular Formula
C13H15NO3
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- Product Description
- Case Study
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- Synthetic Use
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Specification
Synonyms
214610-10-3, TERT-BUTYL 2-OXOINDOLINE-1-CARBOXYLATE, SureCN2419240, CTK0J7492, MolPort-005-940-191, ZINC14517214, AKOS015964540, tert-butyl 2-oxo-1-indolinecarboxylate, AK120578, AM803515, KB-260332, A815394, 2-oxo-3H-indole-1-carboxylic acid tert-butyl ester, tert-butyl 2-oxidanylidene-3H-indole-1-carboxylate, 2-oxo-1,3-dihydro-indole-1-carboxylic acid tert-butyl ester, 2-OXO-2,3-DIHYDRO-INDOLE-1-CARBOXYLIC ACID TERT-BUTYL ESTER, 1H-Indole-1-carboxylic acid, 2,3-dihydro-2-oxo-, 1,1-dimethylethyl ester
IUPAC Name
tert-butyl 2-oxo-3H-indole-1-carboxylate
SMILES
CC(C)(C)OC(=O)N1C(=O)CC2=CC=CC=C21
InChI Key
UZMPOHKOMYCYCZ-UHFFFAOYSA-N
Exact Mass
233.10500
H-Bond Acceptor
3
H-Bond Donor
0
Upstream Synthesis Route 1
- 59-48-3
- 24424-99-5
- 214610-10-3
Reference: [1]Akai, Shuji; Tsujino, Toshiaki; Naka, Tadaatsu; Tanimoto, Kouichi; Kita, Yasuyuki
[Tetrahedron Letters, 2001, vol. 42, # 41, p. 7315 - 7317]
Downstream Synthesis Route 1
- 214610-10-3
- 304876-29-7
Reference: [1] ACS Medicinal Chemistry Letters, 2018, vol. 9, # 2, p. 94 - 97
Downstream Synthesis Route 2
- 50-00-0
- 214610-10-3
- 374898-43-8
Reference: [1]Akai, Shuji; Tsujino, Toshiaki; Naka, Tadaatsu; Tanimoto, Kouichi; Kita, Yasuyuki
[Tetrahedron Letters, 2001, vol. 42, # 41, p. 7315 - 7317]
[2]Akai, Shuji; Tsujino, Toshiaki; Akiyama, Emi; Tanimoto, Kouichi; Naka, Tadaatsu; Kita, Yasuyuki
[Journal of Organic Chemistry, 2004, vol. 69, # 7, p. 2478 - 2486]
[3]Shi, Weihua; Jiang, Zhigan; He, Haiying; Xiao, Fubiao; Lin, Fusen; Sun, Ya; Hou, Lijuan; Shen, Liang; Han, Lixia; Zeng, Minggao; Lai, Kunmin; Gu, Zhengxian; Chen, Xinsheng; Zhao, Tao; Guo, Li; Yang, Chun; Li, Jian; Chen, Shuhui
[ACS Medicinal Chemistry Letters, 2018, vol. 9, # 2, p. 94 - 97]
Downstream Synthesis Route 3
- 214610-10-3
- 74-88-4
- 632324-67-5
Reference: [1]Moody, Christopher J.; Slawin, Alexandra M.Z.; Willows, David
[Organic and Biomolecular Chemistry, 2003, vol. 1, # 15, p. 2716 - 2722]
[2]Koshizawa, Tomoaki; Morimoto, Toshiharu; Watanabe, Gen; Watanabe, Toshiaki; Yamasaki, Nao; Sawada, Yoshikazu; Fukuda, Tomoaki; Okuda, Ayumu; Shibuya, Kimiyuki; Ohgiya, Tadaaki
[Bioorganic and Medicinal Chemistry Letters, 2017, vol. 27, # 15, p. 3249 - 3253]
[3]Current Patent Assignee: ALEMBIC PHARMACEUTICALS LIMITED - WO2021/220120, 2021, A1
Location in patent: Paragraph 215
[4]Li, Honghe; Yan, Xiaoqiang; Zhang, Jitan; Guo, Weicong; Jiang, Jijun; Wang, Jun
[Angewandte Chemie - International Edition, 2019, vol. 58, # 20, p. 6732 - 6736][Angew. Chem., 2019, vol. 131, # 20, p. 6804 - 6808,5]
[5]Current Patent Assignee: CSPC PHARMACEUTICAL GROUP LIMITED - EP3632910, 2020, A1
Location in patent: Paragraph 0231
* For details of the synthesis route, please refer to the original source to ensure accuracy.
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