HCID 69818591、化合物 → HCID 69818136、化合物

HRID 2417441ノート

反応式

HRID 2417441 の反応式
C([N:8]([C@H:20]([CH2:41][OH:42])[CH2:21][C:22]1[CH:27]=[CH:26][C:25]([NH:28][C:29](=[O:40])[C:30]2[CH:39]=[CH:38][C:33]([C:34]([NH:36][CH3:37])=[O:35])=[CH:32][CH:31]=2)=[CH:24][CH:23]=1)[CH2:9][C@H:10]([OH:19])[CH2:11][O:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)C1C=CC=CC=1>CO.[Pd]>[OH:42][CH2:41][C@@H:20]([NH:8][CH2:9][C@H:10]([OH:19])[CH2:11][O:12][C:13]1[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=1)[CH2:21][C:22]1[CH:23]=[CH:24][C:25]([NH:28][C:29](=[O:40])[C:30]2[CH:39]=[CH:38][C:33]([C:34]([NH:36][CH3:37])=[O:35])=[CH:32][CH:31]=2)=[CH:26][CH:27]=1

参加物

4

実験手順

To a solution of N1-[4-[(2S)-2-[N-benzyl-N-[(2S)-2-hydroxy-3-phenoxypropyl]amino]-3-hydroxypropyl]phenyl]-N4-methylterephthalamide (14.0 mg) in methanol (0.5 ml) was added 10% palladium on activated carbon (50% wet, 14.0 mg) and the mixture was hydrogenated at 1 atm for 3 hours. The catalyst was filtered off and washed with methanol. The filtrate was concentrated in vacuo to give N1-[4-[(2S)-3-hydroxy-2-[[(2S)-2-hydroxy-3-phenoxypropyl]amino]propyl]-phenyl]-N4-methylterephthalamide (9.7 mg) as a white solid.

後処理

  1. filtrationThe catalyst was filtered off
  2. washwashed with methanol
  3. concentrationThe filtrate was concentrated in vacuo

出典と根拠

ORDレコード
ord-21ef1227c4dd429a9ee68f42346dd51a
出典データセット
uspto-grants-2004_11
特許番号
US06826033B2

反応ノート

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