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Hydrochloric Acid → HCID 22691363, 화합물

HRID 1876284
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인쇄 미리보기

반응식

HRID 1876284 반응식
Cl.C(OC([N:9]1[CH2:13][CH2:12][CH2:11][C@H:10]1[C:14](=[O:26])[NH:15][CH2:16][CH2:17][C:18]1[CH:23]=[CH:22][C:21]([O:24][CH3:25])=[CH:20][CH:19]=1)=O)(C)(C)C.C(OC)(C)(C)C>O1CCOCC1>[CH3:25][O:24][C:21]1[CH:22]=[CH:23][C:18]([CH2:17][CH2:16][NH:15][C:14]([C@@H:10]2[CH2:11][CH2:12][CH2:13][NH:9]2)=[O:26])=[CH:19][CH:20]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 15413tert-Butyl methyl etherHCID 36760427HCID 36760427, 화합물

생성물 1

HCID 22691363HCID 22691363, 화합물

시약·촉매·용매 1

HCID 312751,4-Dioxane용매2회

실험 절차

4N HCl solution in 41 ml of dioxane is added to a fine suspension of 16.78 g of (S)-2-[2-(4-Methoxy-phenyl)-ethylcarbamoyl]-pyrrolidine-1-carboxylic acid tert-butyl ester in 40 ml of dioxane. After stirring under poor cooling with an ice-bath for 2.5 hours, solvent is evaporated, the residue obtained is cooled over night at 0° and resulting crystals are stirred with 150 ml of tert-butylmethylether, filtered and dried to yield the title compound.

후처리

  1. temperatureunder poor cooling with an ice-bath for 2.5 hours
  2. customsolvent is evaporated
  3. customthe residue obtained
  4. temperatureis cooled over night at 0°
  5. customresulting crystals
  6. filtrationfiltered
  7. customdried

출처 및 근거

ORD 기록
ord-6beae03c261a473995f267f8038dde71
출처 데이터셋
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08309596B2

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