(R)-2-BOC-amino-3-(4-methoxy-benzylsulfanyl)-propionic acid → (R)-2-Amino-3-(4-methoxy-benzylsulfanyl)propionic acid methyl ester

HRID 1045836

反応式

HRID 1045836 の反応式
[C:1]([C@@:8]([NH2:23])([CH2:12][S:13][CH2:14][C:15]1[CH:20]=[CH:19][C:18]([O:21][CH3:22])=[CH:17][CH:16]=1)C(O)=O)([O:3][C:4](C)(C)C)=[O:2]>CO>[CH3:4][O:3][C:1](=[O:2])[C@@H:8]([NH2:23])[CH2:12][S:13][CH2:14][C:15]1[CH:20]=[CH:19][C:18]([O:21][CH3:22])=[CH:17][CH:16]=1

参加物

3

反応物 1

HCID 68486000(R)-2-BOC-amino-3-(4-methoxy-benzylsulfanyl)-propionic acid

生成物 1

HCID 14390800(R)-2-Amino-3-(4-methoxy-benzylsulfanyl)propionic acid methyl ester

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

(R)-2-BOC-amino-3-(4-methoxy-benzylsulfanyl)-propionic acid prepared in Step B of Preparation 27 and methanol were reacted according to the same procedure as Preparation 30 to give the title compound.

後処理

  1. customwere reacted
  2. customaccording to the same procedure as Preparation 30

出典と根拠

ORDレコード
ord-5c38a89ea34b4005a18362e05e865073
出典データセット
uspto-grants-2013_10
特許番号
US08569307B2

関連ノート

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