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HCID 58293367, 화합물 → 3-Methyl-1,6-diazaspiro[3.4]octane-1-carboxylic acid tert-butyl ester

HRID 1912433
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HRID 1912433 반응식
[C:1]([O:5][C:6]([N:8]1[C:11]2([CH2:15][CH2:14][N:13](CC3C=CC=CC=3)[CH2:12]2)[CH:10]([CH3:23])[CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2]>O1CCCC1.CO.[C+4].[OH-].[Pd+2].[OH-].[OH-].[OH-].[OH-].[OH-]>[C:1]([O:5][C:6]([N:8]1[C:11]2([CH2:15][CH2:14][NH:13][CH2:12]2)[CH:10]([CH3:23])[CH2:9]1)=[O:7])([CH3:4])([CH3:2])[CH3:3]
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참가 물질

4

반응물 1

HCID 58293367HCID 58293367, 화합물

생성물 1

HCID 582933013-Methyl-1,6-diazaspiro[3.4]octane-1-carboxylic acid tert-butyl ester수율 102.1%

시약·촉매·용매 2

HCID 178420936HCID 178420936, 화합물촉매HCID 21899815MeOH tetrahydrofuran용매

실험 절차

To a solution of an optically-active compound of 6-benzyl-3-methyl-1,6-diazaspiro[3.4]octane-1-carboxylic acid tert-butyl ester (10.0 g) in tetrahydrofuran/methanol (50 ml/50 ml) was added 20% palladium hydroxide carbon (2.0 g), and the mixture was hydrogenated under 4 atmospheres for 24 hours. The mixture was filtered through Celite, and the filtrate was concentrated under reduced pressure to give the titled compound (7.3 g).

후처리

  1. filtrationThe mixture was filtered through Celite
  2. concentrationthe filtrate was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-710611c8847a433e9925e66cbc46a46c
출처 데이터셋
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08609647B2

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