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Water → cis 4-Thiocyanatomethyl-3-phthalimido-2-oxo-azetidine

HRID 1199587
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인쇄 미리보기

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HRID 1199587 반응식
[S-:1][C:2]#[N:3].[K+].I[CH2:6][C@H:7]1[NH:10][C:9](=[O:11])[C@H:8]1[N:12]1[C:16](=[O:17])[C:15]2=[CH:18][CH:19]=[CH:20][CH:21]=[C:14]2[C:13]1=[O:22].O>CN(C)C=O>[S:1]([CH2:6][C@H:7]1[NH:10][C:9](=[O:11])[C@H:8]1[N:12]1[C:16](=[O:17])[C:15]2=[CH:18][CH:19]=[CH:20][CH:21]=[C:14]2[C:13]1=[O:22])[C:2]#[N:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 516872Potassium thiocyanateHCID 13424465cis 4-Iodomethyl-3-phthalimido-2-oxo-azetidine

생성물 1

HCID 86743759cis 4-Thiocyanatomethyl-3-phthalimido-2-oxo-azetidine

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

1.5 g of potassium thiocyanate were added at 75° C. with stirring to a mixture of 1.78 g of the product of Step A in 5 ml of dimethylformamide and the mixture was stirred for 31/2 hours and was poured into water. The mixture was vacuum filtered and the product was washed with water and dried. The product was empasted with hot isopropyl ether, vacuum filtered and dried to obtain 1.25 g of racemate of cis 4-thiocyanatomethyl-3-phthalimido-2-oxo-azetidine.

후처리

  1. filtrationfiltered
  2. washthe product was washed with water
  3. customdried
  4. filtrationfiltered
  5. customdried

출처 및 근거

ORD 기록
ord-1d5df9f012c84679bf24573457c7c3e1
출처 데이터셋
uspto-grants-1990_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04900728

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