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Water → HCID 22861115, 화합물

HRID 439892
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HRID 439892 반응식
[C:1]([NH:8][CH2:9][C@H:10]1[CH2:12][C@H:11]1[CH2:13][O:14][N:15]1C(=O)C2C(=CC=CC=2)C1=O)([O:3][C:4]([CH3:7])([CH3:6])[CH3:5])=[O:2].O>C(Cl)Cl>[O:14]([CH2:13][C@H:11]1[CH2:12][C@H:10]1[CH2:9][NH:8][C:1]([O:3][C:4]([CH3:7])([CH3:6])[CH3:5])=[O:2])[NH2:15]
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4

반응물 2

HCID 962WaterHCID 22861110HCID 22861110, 화합물

생성물 1

HCID 22861115HCID 22861115, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

A mixture of 1.5 g (0.00433 mol) of 2-[cis-2-(N-BOC-aminomethyl)-cyclopropylmethoxy]-1H-isoindole-1,3(2H)-dione and 9 ml of hydrazinc hydrate is stirred at room temperature for 1/2 hour. 9 ml of water are then added to the reaction mixture and, after a further 1/2 hour, 50 ml of methylene chloride are added. The reaction mixture is further stirred for another 3 hours, the methylene chloride phase is then separated off and the aqueous phase is washed twice with 30 ml of methylene chloride each time. The combined organic phases are washed with brine, dried over sodium sulfate and evaporated. The oily cis-2-aminoxymethyl-N-BOC-cyclopropylmethylamine thus obtained, Rf value=0.13 (silica gel/ethyl acetate:hexane (1:1)), is dissolved in 18 ml of 3M methanolic hydrochloric acid and the reaction mixture is stirred at room temperature for 1 hour. After addition of diethyl ether and cooling in an ice-bath, the title compound which has crystallized out is filtered off, washed with diethyl ether and dried, m.p. 178°-180° C. (decomp.).

후처리

  1. stirringThe reaction mixture is further stirred for another 3 hours
  2. customthe methylene chloride phase is then separated off
  3. washthe aqueous phase is washed twice with 30 ml of methylene chloride each time
  4. washThe combined organic phases are washed with brine
  5. dry with materialdried over sodium sulfate
  6. customevaporated

출처 및 근거

ORD 기록
ord-e2946d402f0f4619b6396b7f7d7f9a4e
출처 데이터셋
uspto-grants-1996_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05516806

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