1-Boc-indoline-5-boronic acid pinacol ester

• CAS: 837392-67-3
• Catalog Number: ACM837392673
• Category: Other Products; Other
• Molecular Weight: 345.2445
• Molecular Formula: C19H28BNO4
• Synonyms: 1-Boc-indoline-5-boronic acid pinacol ester, 837392-67-3, TERT-BUTYL 5-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)INDOLINE-1-CARBOXYLATE, SureCN868675, AGN-PC-01W82V, MolPort-020-003-396, FD6054, AB65598, KB-40805, A-3817, 1-(TERT-BUTOXYCARBONYL)-5-INDOLINEBORONIC ACID PINACOL ESTER, 1,1-DIMETHYLETHYL 5-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-2,3-DIHYDRO-1H-INDOLE-1-CARBOXYLATE, 1H-INDOLE-1-CARBOXYLIC ACID, 2,3-DIHYDRO-5-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-, 1,1-DIMETHYLETHYL ESTER, 2,3-Dihydro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-1-carboxylic Acid 1,1-Dimethylethyl Ester, 2,3-Dihydro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-1-carboxylic Acid tert-Butyl Ester, 5-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)-2,3-dihydro-indole-1-carboxylic acid tert-butyl ester, tert-butyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,3-dihydroindole-1-carboxylate
• IUPAC Name: tert-butyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,3-dihydroindole-1-carboxylate
• Canonical SMILES: B1(OC(C(O1)(C)C)(C)C)C2=CC3=C(C=C2)N(CC3)C(=O)OC(C)(C)C
• InChI Key: OOORQXGLIKPNDK-UHFFFAOYSA-N
• Exact Mass: 345.21100
• H-Bond Acceptor: 4
• H-Bond Donor: 0
• MDL Number: MFCD12408237
• Size: 100mg,250mg,500mg,1g,5g,25g

Custom Reviews

June 16, 2023

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Good application in organic synthesis
The pinacol compound prepared by 1-boc-indoline-5-boronic acid pinacol ester has high conversion rate.

Synthetic Use

Upstream Synthesis Route 1

• 261732-38-1
• 73183-34-3

• 837392-67-3

Reference: [1]Journal of Medicinal Chemistry,2012,vol. 55,p. 7193 - 7207

Downstream Synthesis Route 1

• 837392-67-3

• 1062174-44-0

Reference: [1] Patent: WO2012/103806, 2012, A1, . Location in patent: Page/Page column 48

Downstream Synthesis Route 2

• 837392-67-3

• 1337531-36-8

Reference: [1] Journal of Medicinal Chemistry, 2012, vol. 55, # 16, p. 7193 - 7207

Downstream Synthesis Route 3

• 837392-67-3
• 79544-29-9

• 1337532-62-3

Reference: [1]Patent: WO2011/119663,2011,A1 .Location in patent: Page/Page column 87

Downstream Synthesis Route 4

• 799293-73-5
• 837392-67-3

• 1337532-93-0

Reference: [1]Journal of Medicinal Chemistry,2012,vol. 55,p. 7193 - 7207
[2]Patent: WO2011/119663,2011,A1 .Location in patent: Page/Page column 128-129
[3]Patent: WO2011/119663,2011,A1 .Location in patent: Page/Page column 215

* For details of the synthesis route, please refer to the original source to ensure accuracy.