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Hydrogen Bromide → 2-Bromo-5-methyl-4,5,6,7-tetrahydrothiazolo(5,4-c)pyridine

HRID 557240
ノート
印刷プレビュー

反応式

HRID 557240 の反応式
N[C:2]1[S:3][C:4]2[CH2:5][N:6]([CH3:11])[CH2:7][CH2:8][C:9]=2[N:10]=1.[BrH:12].N([O-])=O.[Na+].[OH-].[Na+]>O>[Br:12][C:2]1[S:3][C:4]2[CH2:5][N:6]([CH3:11])[CH2:7][CH2:8][C:9]=2[N:10]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 260Hydrogen BromideHCID 14798Sodium HydroxideHCID 23979985-methyl-4H,5H,6H,7H-[1,3]thiazolo[5,4-c]pyridin-2-amineHCID 23668193Sodium Nitrite

生成物 1

HCID 111723352-Bromo-5-methyl-4,5,6,7-tetrahydrothiazolo(5,4-c)pyridine

試薬・触媒・溶媒 1

HCID 962Water溶媒2 回

反応条件

温度
30 °C

実験手順

2-Amino-5-methyl-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridine (600.0 g) was suspended in water (6.0 L), and 48% hydrobromic acid (4.2 L) was added dropwise thereto at 5 to 15° C. A solution of sodium nitrite (367.2 g) in water (1.8 L) was added dropwise thereto at 0 to 5° C. over 1.5 hours, and the reaction mixture was heated to 30° C., followed by stirring for 24 hours. The resultant mixture was made strongly basic (pH 12.5) with 5N aqueous sodium hydroxide (6.0 L). The aqueous layer was extracted with toluene twice (12.0 L, 6.0 L), and the toluene layers were combined. The combined toluene layer was dried over sodium sulfate anhydrate (1202.0 g), and after any insoluble material was filtered off, the mother liquor was concentrated at 40° C. under reduced pressure, to thereby give 557.6 g of the title compound.

後処理

  1. customat 5 to 15° C
  2. extractionThe aqueous layer was extracted with toluene twice (12.0 L, 6.0 L)
  3. dry with materialThe combined toluene layer was dried over sodium sulfate anhydrate (1202.0 g)
  4. filtrationafter any insoluble material was filtered off
  5. concentrationthe mother liquor was concentrated at 40° C. under reduced pressure

出典と根拠

ORDレコード
ord-75ba8a71c6724b758b23d5cbec286bb8
出典データセット
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08058440B2

反応ノート

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