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Bromoacetic Acid → 2-Benzyloxycarbonylamino-3-(bromoactyl-prop-2-ynyl-amino)-propionic acid methyl ester

HRID 1432922
ノート
印刷プレビュー

反応式

HRID 1432922 の反応式
C1CCC(N=C=NC2CCCCC2)CC1.[Br:16][CH2:17][C:18](O)=[O:19].[CH3:21][O:22][C:23](=[O:41])[CH:24]([NH:30][C:31]([O:33][CH2:34][C:35]1[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=1)=[O:32])[CH2:25][NH:26][CH2:27][C:28]#[CH:29]>C(Cl)Cl.CCOCC>[CH3:21][O:22][C:23](=[O:41])[CH:24]([NH:30][C:31]([O:33][CH2:34][C:35]1[CH:36]=[CH:37][CH:38]=[CH:39][CH:40]=1)=[O:32])[CH2:25][N:26]([C:18](=[O:19])[CH2:17][Br:16])[CH2:27][C:28]#[CH:29]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 6227Bromoacetic AcidHCID 10868DicyclohexylcarbodiimideHCID 544236402-Benzyloxycarbonylamino-3-(prop-2-ynylamino)-propionic acid methyl ester

生成物 1

HCID 1317277242-Benzyloxycarbonylamino-3-(bromoactyl-prop-2-ynyl-amino)-propionic acid methyl ester収率 47.9%

試薬・触媒・溶媒 2

HCID 3283Diethyl Ether溶媒
HCID 6344
Dichloromethane
溶媒

実験手順

DCC (2.27 g, 11.0 mmol) and bromoacetic acid (1.48 g, 10.7 mmol) is added to a solution of 2-benzyloxycarbonylamino-3-(prop-2-ynylamino)-propionic acid methyl ester (3.10 g, 10.7 mmol) in CH2Cl2 at RT. The mixture is stirred overnight then diluted with ether. The white solid which precipitates out is filtered and the filtrate is concentrated to give a yellow oil. The crude product is purified by chromatography eluting with a gradient of 40% EtOAc/hexanes to 50% EtOAc/hexanes to yield the title product (2.1 g, 5.12 mmol) as an oil. 1H NMR (CDCl3, 300 MHz) δ7.30 (m, 5H), 5.70 (d, 1H), 5.10 (s, 2H), 4.63 (m, 1H), 4.15 (d, 2H), 4.00 (m, 1H), 3.80 (s, 3H), 3.75 (s, 2H), 3.70 (dd, 1H), 2.27 (bs, 1H). Ion spray MS, [M+H]+=411, 413, Br pattern.

後処理

  1. customThe white solid which precipitates out
  2. filtrationis filtered
  3. concentrationthe filtrate is concentrated
  4. customto give a yellow oil
  5. customThe crude product is purified by chromatography
  6. washeluting with a gradient of 40% EtOAc/hexanes to 50% EtOAc/hexanes

出典と根拠

ORDレコード
ord-356294f83e544092bde454bc39068ad5
出典データセット
uspto-grants-2009_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07612075B2

反応ノート

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