alpha-Bromo-o-fluorotoluene → 2-[[2-amino-5-[[(2-fluorophenyl)methyl]thio]thiazolo[4,5-d]pyrimidin-7-yl]amino]-(2R)-1-propanol

HRID 1006512노트

반응식

HRID 1006512 반응식
[F:1][C:2]1[CH:9]=[CH:8][CH:7]=[CH:6][C:3]=1[CH2:4]Br.[NH2:10][C:11]1[S:12][C:13]2[C:18]([NH:19][C@H:20]([CH3:23])[CH2:21][OH:22])=[N:17][C:16]([SH:24])=[N:15][C:14]=2[N:25]=1.C(N(C(C)C)CC)(C)C>CS(C)=O.CN1CCCC1=O>[NH2:10][C:11]1[S:12][C:13]2[C:18]([NH:19][C@H:20]([CH3:23])[CH2:21][OH:22])=[N:17][C:16]([S:24][CH2:4][C:3]3[CH:6]=[CH:7][CH:8]=[CH:9][C:2]=3[F:1])=[N:15][C:14]=2[N:25]=1

참가 물질

5

반응물 3

HCID 67968alpha-Bromo-o-fluorotolueneHCID 81531DiisopropylethylamineHCID 178461804HCID 178461804, 화합물

생성물 1

HCID 235198222-[[2-amino-5-[[(2-fluorophenyl)methyl]thio]thiazolo[4,5-d]pyrimidin-7-yl]amino]-(2R)-1-propanol수율 35%

시약·촉매·용매 1

HCID 18784345DMSO N-methylpyrrolidinone용매

실험 절차

2-fluorobenzylbromide (0.369 g) was added portionwise to a solution of the product of example 32 step b) (0.5 g) and diisopropylethylamine (0.26 g) in DMSO/N-methylpyrrolidinone (4 ml/0.5 ml) at 50° C. and stirring maintained for 1 h. The mixture was partitioned between H2O (200 ml) and EtOAc (120 ml). The organics were recovered and washed flier with H2O (200 ml), dried over MgSO4 and concentrated onto silica gel. The subtitle compound was purified by flash chromatography using DCM then EtOAc as eluents to yield a white solid (245 mg, 35%).

후처리

  1. temperaturemaintained for 1 h
  2. customThe mixture was partitioned between H2O (200 ml) and EtOAc (120 ml)
  3. customThe organics were recovered
  4. washwashed flier with H2O (200 ml)
  5. dry with materialdried over MgSO4
  6. concentrationconcentrated onto silica gel
  7. customThe subtitle compound was purified by flash chromatography

출처 및 근거

ORD 기록
ord-bcd0ebf3d84c48b8862abb3994de21c2
출처 데이터셋
uspto-grants-2004_09
특허 번호
US06790850B1

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