Sodium cyanoborohydride → Tert-butyl {3-[2-(1-hydroxy-1-propylbutyl)phenylamino]-1,1-dimethylpropyl}carbamate

HRID 2223121노트

반응식

HRID 2223121 반응식
C([BH3-])#N.[Na+].[NH2:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=1[C:12]([OH:19])([CH2:16][CH2:17][CH3:18])[CH2:13][CH2:14][CH3:15].[CH3:20][C:21]([NH:26][C:27](=[O:33])[O:28][C:29]([CH3:32])([CH3:31])[CH3:30])([CH3:25])[CH2:22][CH:23]=O>CO.CC(O)=O.CCOC(C)=O>[C:29]([O:28][C:27](=[O:33])[NH:26][C:21]([CH3:25])([CH3:20])[CH2:22][CH2:23][NH:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=1[C:12]([OH:19])([CH2:16][CH2:17][CH3:18])[CH2:13][CH2:14][CH3:15])([CH3:32])([CH3:31])[CH3:30]

참가 물질

7

반응물 3

HCID 5003444Sodium cyanoborohydrideHCID 11788901tert-butyl N-(2-methyl-4-oxobutan-2-yl)carbamateHCID 210728384-(2-Aminophenyl)heptan-4-ol

생성물 1

HCID 86600980Tert-butyl {3-[2-(1-hydroxy-1-propylbutyl)phenylamino]-1,1-dimethylpropyl}carbamate

시약·촉매·용매 3

HCID 176Acetic Acid용매HCID 887Methanol용매HCID 8857Ethyl Acetate용매

실험 절차

1.40 g (22.27 mmol) of sodium cyanoborohydride is added to a solution of 3.10 g (14.05 mmol) of 4-(2-aminophenyl)heptan-4-ol and 3.60 g (17.88 mmol) of tert-butyl (1,1-dimethyl-3-oxopropyl)carbamate in MeOH (40 mL) and AcOH (6 mL). The mixture is stirred for 16 hours at RT, diluted with EtOAc, and washed with 0.5 M aqueous KHSO4 and saturated aqueous NaCl, dried with sodium sulfate, and evaporated down in vacuo. The crude product is used in the next reaction step without any further purification. Yield: 6.00 g (quantitative yield).

후처리

  1. washwashed with 0.5 M aqueous KHSO4 and saturated aqueous NaCl
  2. dry with materialdried with sodium sulfate
  3. customevaporated down in vacuo
  4. customThe crude product is used in the next reaction step without any further purification

출처 및 근거

ORD 기록
ord-04cc95a95923471ea3f38993d19e9608
출처 데이터셋
uspto-grants-2008_05
특허 번호
US07375104B2

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