Hydrochloric Acid → HCID 19957051、化合物

HRID 55004ノート

反応式

HRID 55004 の反応式
[ClH:1].Cl.C[O:4][C:5]1[CH:10]=[CH:9][C:8]([CH:11]2[C:17]3[CH:18]=[CH:19][CH:20]=[CH:21][C:16]=3[CH2:15][N:14]([CH3:22])[C:13]([CH2:23][CH2:24][C:25]3[CH:30]=[CH:29][N:28]=[CH:27][CH:26]=3)=[N:12]2)=[CH:7][CH:6]=1.C([O-])(=O)/C=C/C([O-])=O.B(Br)(Br)Br.Cl>C(Cl)Cl>[ClH:1].[ClH:1].[OH:4][C:5]1[CH:10]=[CH:9][C:8]([CH:11]2[C:17]3[CH:18]=[CH:19][CH:20]=[CH:21][C:16]=3[CH2:15][N:14]([CH3:22])[C:13]([CH2:23][CH2:24][C:25]3[CH:26]=[CH:27][N:28]=[CH:29][CH:30]=3)=[N:12]2)=[CH:7][CH:6]=1

参加物

6

実験手順

To a mixture of 4,5-dihydro-1-(4-methoxyphenyl)-4-methyl-3-[2-(4-pyridyl)ethyl]-1H-2,4-benzodiazepine dihydrochloride (3.81 g, 8.6 mmol, prepared from the fumarate of Example 398 by standard procedures) in CH2Cl2 (40 mL) in an ice-bath under N2 was added boron tribromide (17.2 mL, 1M in CH2Cl2). The mixture was stirred for 3 hours, 2N HCl was added and the mixture was stirred for 1/2 hour. The layers were separated, the aqueous layer was extracted with CH2Cl2 and the combined organic layers were washed with 2N HCl. The organic layer was treated with saturated Na2CO3 and the product which precipitates was collected by filtration to afford 3.06 g (83%) of 4,5-dihydro-1-(4-hydroxyphenyl)-4-methyl-3-[2-(4-pyridyl)ethyl]-1H-2,4-benzodiazepine dihydrochloride, m.p. 258°-259° C. after recrystallization from methanol/ether.

後処理

  1. stirringthe mixture was stirred for 1/2 hour
  2. customThe layers were separated
  3. extractionthe aqueous layer was extracted with CH2Cl2
  4. washthe combined organic layers were washed with 2N HCl
  5. additionThe organic layer was treated with saturated Na2CO3
  6. customthe product which precipitates
  7. filtrationwas collected by filtration

出典と根拠

ORDレコード
ord-a4b8f0eb5792475cbef6c6c77c06bd3c
出典データセット
uspto-grants-1997_04
特許番号
US05624922

反応ノート

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