Ammonia → (R)-5-(5-Bromo-2-fluoro-phenyl)-5-methyl-5,6-dihydro-2H-[1,4]oxazin-3-ylamine

HRID 1946914노트

반응식

HRID 1946914 반응식
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([F:16])=[C:6]([C@@:8]2([CH3:15])[NH:13][C:12](=S)[CH2:11][O:10][CH2:9]2)[CH:7]=1.[NH3:17].C(OO)(C)(C)C>CO.O>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([F:16])=[C:6]([C@:8]2([CH3:15])[CH2:9][O:10][CH2:11][C:12]([NH2:17])=[N:13]2)[CH:7]=1

참가 물질

6

반응물 3

HCID 222AmmoniaHCID 6410tert-Butyl hydroperoxideHCID 86668499(R)-5-(5-bromo-2-fluoro-phenyl)-5-methyl-morpholine-3-thione

생성물 1

HCID 58155238(R)-5-(5-Bromo-2-fluoro-phenyl)-5-methyl-5,6-dihydro-2H-[1,4]oxazin-3-ylamine

시약·촉매·용매 2

HCID 887Methanol용매2회HCID 962Water용매

실험 절차

A pressure tube was charged with a solution of (R)-5-(5-bromo-2-fluoro-phenyl)-5-methyl-morpholine-3-thione (1.93 g, 6.3 mmol) in methanol (195 ml). A solution of ammonia in methanol (7M, 54 ml, 381 mmol) and an aqueous solution of tert-butyl hydroperoxide (70%, 8.17 g, 63.4 mmol) were added. The tube was sealed and the reaction mixture was stirred overnight at room temperature for 21 hours. For the workup, the reaction mixture was diluted with water and extracted three times with dichloromethane. The combined organic layers were washed with brine, dried over sodium sulphate and evaporated. The crude product was purified by chromatography on an Isolute flash NH2 column using dichloromethane as the eluent. The (R)-5-(5-bromo-2-fluoro-phenyl)-5-methyl-5,6-dihydro-2H-[1,4]oxazin-3-ylamine was obtained as an off-white gum (1.42 g, 62% of theory). MS (ISP): m/z=287.1 [M+H]+, 289.0 [M+2+H]+.

후처리

  1. customThe tube was sealed
  2. extractionextracted three times with dichloromethane
  3. washThe combined organic layers were washed with brine
  4. dry with materialdried over sodium sulphate
  5. customevaporated
  6. customThe crude product was purified by chromatography on an Isolute flash NH2 column

출처 및 근거

ORD 기록
ord-5c4afc2b2ed64f9faa1aee23992df241
출처 데이터셋
uspto-grants-2013_03
특허 번호
US08399459B2

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