Sodium → rel-1,1-Dimethylethyl N-[(2R,3S)-2-methyl-4-oxo-3-azetidinyl]carbamate

HRID 867647노트

반응식

HRID 867647 반응식
[Na].[C:2]([O:6][C:7]([NH:9][C@H:10]1[C@@H:13]([CH3:14])[N:12](OC)[C:11]1=[O:17])=[O:8])([CH3:5])([CH3:4])[CH3:3]>N.O1CCCC1>[C:2]([O:6][C:7]([NH:9][C@H:10]1[C@@H:13]([CH3:14])[NH:12][C:11]1=[O:17])=[O:8])([CH3:5])([CH3:3])[CH3:4]

참가 물질

5

반응물 2

HCID 5360545SodiumHCID 57291996Carbamic acid, (1-methoxy-2-methyl-4-oxo-3-azetidinyl)-, 1,1-dimethylethyl ester, (2R-cis)-

생성물 1

HCID 57285608rel-1,1-Dimethylethyl N-[(2R,3S)-2-methyl-4-oxo-3-azetidinyl]carbamate수율 94.4%

시약·촉매·용매 2

HCID 222Ammonia용매HCID 8028Tetrahydrofuran용매2회

실험 절차

Sodium (1.35 g) is dissolved in about 300 ml of liquid ammonia at -50° C. and 5.87 g of (3S-cis)-3-t-Butoxycarbonylamino-1-methoxy-4-methylazetidinone in 35 ml tetrahydrofuran is added dropwise via syringe. An additional 10 ml of tetrahydrofuran is used for rinsing. Near the end of the addition about 100 mg of additional sodium is added. The mixture is stirred for five more minutes, then quenched by adding 3.35 g of solid ammonium chloride in one portion. Ammonia is blown off with a nitrogen stream and 250 ml of ethyl acetate is added to the residue. After filtration and washing the solid with ethyl acetate, the combined filtrate is stripped of solvent to give 4.82 g of the title compound.

후처리

  1. washfor rinsing
  2. additionNear the end of the addition about 100 mg of additional sodium
  3. additionis added
  4. customquenched
  5. additionby adding 3.35 g of solid ammonium chloride in one portion
  6. additionis added to the residue
  7. filtrationAfter filtration
  8. washwashing the solid with ethyl acetate

출처 및 근거

ORD 기록
ord-4dcbf96705da4cbca5f545ae1c60c455
출처 데이터셋
uspto-grants-1988_10
특허 번호
US04775670

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