Sodium Hydroxide → (3S,4aS,8aS)-2-((2R,3S)-3-amino-2-hydroxy-4-phenylbutyl)-N-tert-butyldecahydroisoquinoline-3-carboxamide

HRID 233342노트

반응식

HRID 233342 반응식
[CH2:1]([C@H:8]([NH:30]C(=O)OC)[C@H:9]([OH:29])[CH2:10][N:11]1[C@H:20]([C:21](=[O:28])[NH:22]OC(C)(C)C)[CH2:19][C@H:18]2[C@H:13]([CH2:14][CH2:15][CH2:16][CH2:17]2)[CH2:12]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[OH-].[Na+]>C(O)C.O>[NH2:30][C@@H:8]([CH2:1][C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1)[C@H:9]([OH:29])[CH2:10][N:11]1[C@H:20]([C:21]([NH:22][C:2]([CH3:7])([CH3:3])[CH3:1])=[O:28])[CH2:19][C@H:18]2[C@H:13]([CH2:14][CH2:15][CH2:16][CH2:17]2)[CH2:12]1

참가 물질

5

반응물 2

HCID 14798Sodium HydroxideHCID 86750132methyl(1S,2R)-[1-benzyl-3-[(3S,4aS,8aS)-3-tert-butoxycarbamoyl-octahydro-isoquinolin-2-yl]-2-hydroxy-propyl]-carbamate

생성물 1

HCID 9865804(3S,4aS,8aS)-2-((2R,3S)-3-amino-2-hydroxy-4-phenylbutyl)-N-tert-butyldecahydroisoquinoline-3-carboxamide수율 202.4%

시약·촉매·용매 2

HCID 702Ethanol용매HCID 962Water용매2회

실험 절차

A suspension of 41.37 g of methyl (1S,2R)-[1-benzyl-3-[(3S,4aS,8aS)-3-tert-butoxycarbamoyl-octahydro-isoquinolin-2-yl]-2-hydroxy-propyl]-carbamate and 23.0 g of sodium hydroxide in 90 ml of ethanol and 90 ml of water was heated at reflux for 3.5 hours, diluted with 45 ml of water and cooled to 22°, and the separated solid was filtered off, washed with a 1:4 mixture of ethanol/water and dried, there being obtained 35.35 g (98%) of pure 2-[3 (S)-amino-2(R)-hydroxy-4-phenyl-butyl]-N-tert.butyldecahydro-(4aS,8aS)-isoquinoline-3(S)-carboxamide, m.p. 173°-175° C. IR (KBr): 3435 m, hr. (NH, OH), 1665s (C=O), 1562 m (amide II).

후처리

  1. temperaturewas heated
  2. temperatureat reflux for 3.5 hours
  3. temperaturecooled to 22°
  4. filtrationthe separated solid was filtered off
  5. washwashed with a 1:4 mixture of ethanol/water
  6. customdried

출처 및 근거

ORD 기록
ord-041ce376798d4b14b0f9f9a78d68b5ee
출처 데이터셋
uspto-grants-1997_01
특허 번호
US05591885

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