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Boron tribromide → 1-(4-Benzo[b]thiophen-2-yl-benzyl)-1,2,3,4-tetrahydro-isoquinoline-6,7-diol hydrobromide

HRID 1295414
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1295414
C(OC([N:8]1[CH2:17][CH2:16][C:15]2[C:10](=[C:11](C)[C:12]([O:20]C)=[C:13]([O:18]C)[CH:14]=2)[CH:9]1[CH2:23][C:24]1[CH:29]=[CH:28][C:27]([C:30]2[S:34][C:33]3[CH:35]=[CH:36][CH:37]=[CH:38][C:32]=3[CH:31]=2)=[CH:26][CH:25]=1)=O)(C)(C)C.B(Br)(Br)[Br:40]>ClCCl>[BrH:40].[S:34]1[C:30]([C:27]2[CH:28]=[CH:29][C:24]([CH2:23][CH:9]3[C:10]4[C:15](=[CH:14][C:13]([OH:18])=[C:12]([OH:20])[CH:11]=4)[CH2:16][CH2:17][NH:8]3)=[CH:25][CH:26]=2)=[CH:31][C:32]2[CH:38]=[CH:37][CH:36]=[CH:35][C:33]1=2
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Komponenten

4

Edukt 2

HCID 25134Boron tribromideHCID 865909591-(4-benzo[b]thiophen-2-yl-benzyl)-6,7-dimethoxy-8-methyl-3,4-dihydro-1-H-isoquinoline-2-carboxylic acid tert-butyl ester

Produkt 1

HCID 686841711-(4-Benzo[b]thiophen-2-yl-benzyl)-1,2,3,4-tetrahydro-isoquinoline-6,7-diol hydrobromide

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

1-(4-Benzo[b]thiophen-2-yl-benzyl)-1,2,3,4-tetrahydro-isoquinoline-6,7-diol hydrobromide (22) was prepared as follows: To a stirred solution of 0.15 g (0.29 mmole) of 1-(4-benzo[b]thiophen-2-yl-benzyl)-6,7-dimethoxy-8-methyl-3,4-dihydro-1-H-isoquinoline-2-carboxylic acid tert-butyl ester in 10 ml of anhydrous dichloromethane under argon at −70° C., 0.9 ml (3 mol. equiv.) of 1M boron tribromide solution in n-hexanes was added. The stirred mixture was allowed to reach room temperature overnight and the solvents were evaporated under reduced pressure. The residue was dissolved in 10 ml of methanol and, again, the solvent was evaporated under reduced pressure. The solid residue was mixed with 10 ml of ether, separated on a glass filter funnel, washed with ether (3×20 ml) to afford an off-white solid, 130 mg (91%), mp 251-254° C.

Aufarbeitung

  1. customthe solvents were evaporated under reduced pressure
  2. dissolutionThe residue was dissolved in 10 ml of methanol
  3. customagain, the solvent was evaporated under reduced pressure
  4. additionThe solid residue was mixed with 10 ml of ether
  5. customseparated on a glass
  6. filtrationfilter funnel
  7. washwashed with ether (3×20 ml)
  8. customto afford an off-white solid, 130 mg (91%), mp 251-254° C.

Quellen und Nachweise

ORD-Eintrag
ord-531debf6731746739f356754b0f9975c
Quelldatensatz
uspto-grants-2007_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07241774B2

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