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Hydrochloric Acid → 5-Amino-5-methyl-hexahydro-cyclopenta[c]pyrrole-2-carboxylic acid dimethylamide

HRID 1873517
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반응식

HRID 1873517 반응식
[CH3:1][N:2]([CH3:16])[C:3]([N:5]1[CH2:9][CH:8]2[CH2:10][C:11]([N+:14]#[C-])([CH3:13])[CH2:12][CH:7]2[CH2:6]1)=[O:4].Cl>C(O)C>[CH3:16][N:2]([CH3:1])[C:3]([N:5]1[CH2:9][CH:8]2[CH2:10][C:11]([NH2:14])([CH3:13])[CH2:12][CH:7]2[CH2:6]1)=[O:4]
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참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 723389335-Isocyano-5-methyl-hexahydro-cyclopenta[c]pyrrole-2-carboxylic acid dimethylamide

생성물 1

HCID 686275765-Amino-5-methyl-hexahydro-cyclopenta[c]pyrrole-2-carboxylic acid dimethylamide수율 75.7%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a solution of 5-isocyano-5-methyl-hexahydro-cyclopenta[c]pyrrole-2-carboxylic acid dimethylamide 11b (0.388 g, 1.75 mmol) in 15 mL of ethanol was added 0.38 mL of hydrochloric acid (6 N) upon cooling by an ice-water bath. The reaction mixture was warmed up to room temperature and stirred for 1.5 hours. The reaction was monitored by TLC until the disappearance of the starting materials. The mixture was quenched with 20 mL of saturated aqueous sodium carbonate. The mixture was extracted with dichloromethane (50 mL×3). The combined organic extracts were evaporated to dryness. The resulting residue was purified by silica gel column chromatography to obtain the title compound 5-amino-5-methyl-hexahydro-cyclopenta[c]pyrrole-2-carboxylic acid dimethylamide 11c (0.28 g, yield 75.7%) as a yellow oil.

후처리

  1. temperatureupon cooling by an ice-water bath
  2. customThe mixture was quenched with 20 mL of saturated aqueous sodium carbonate
  3. extractionThe mixture was extracted with dichloromethane (50 mL×3)
  4. customThe combined organic extracts were evaporated to dryness
  5. customThe resulting residue was purified by silica gel column chromatography

출처 및 근거

ORD 기록
ord-4b52407effe449379d974d70f5e2dbce
출처 데이터셋
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08304411B2

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