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Glycine → HCID 178455935、化合物

HRID 329552
ノート
印刷プレビュー

反応式

HRID 329552 の反応式
C(O)(C(F)(F)F)=O.[NH2:8][CH2:9][C:10]([OH:12])=[O:11].CCN(C(C)C)C(C)C.C1C=CC2N(O)N=NC=2C=1.C1CCC(N=C=NC2CCCCC2)CC1.[NH:47]([C:77]([O:79][C:80]([CH3:83])([CH3:82])[CH3:81])=[O:78])[C@H:48]([C:66]([NH:68][C@H:69]([C:74](O)=[O:75])[C@H:70]([CH2:72][CH3:73])[CH3:71])=[O:67])[CH2:49][CH2:50][CH2:51][NH:52][C:53](=[NH:65])[NH:54][S:55]([C:58]1[CH:64]=[CH:63][C:61]([CH3:62])=[CH:60][CH:59]=1)(=[O:57])=[O:56]>CN(C=O)C.C(Cl)Cl>[NH:47]([C:77]([O:79][C:80]([CH3:82])([CH3:81])[CH3:83])=[O:78])[C@H:48]([C:66]([NH:68][C@H:69]([C:74]([NH:8][CH2:9][C:10]([OH:12])=[O:11])=[O:75])[C@H:70]([CH2:72][CH3:73])[CH3:71])=[O:67])[CH2:49][CH2:50][CH2:51][NH:52][C:53](=[NH:65])[NH:54][S:55]([C:58]1[CH:64]=[CH:63][C:61]([CH3:62])=[CH:60][CH:59]=1)(=[O:57])=[O:56]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

9

反応物 6

HCID 750GlycineHCID 6422Trifluoroacetic acidHCID 10868DicyclohexylcarbodiimideHCID 757711-HydroxybenzotriazoleHCID 81531DiisopropylethylamineHCID 178455936HCID 178455936、化合物

生成物 1

HCID 178455935
HCID 178455935、化合物

試薬・触媒・溶媒 2

HCID 6228Dimethylformamide溶媒HCID 6344Dichloromethane溶媒2 回

反応条件

温度
0 °C

実験手順

Tripeptide H-Arg(Tos)-Ile-Gly-OFm: The latter dipeptide (14.81 g, 27.3 mmol) was dissolved in DMF (75 mL). TFA.H-Gly-OFm (10.0 g, 27.3 mmol), DIEA (14.3 mL, 81.9 mmol) and HOBt (3.69 g, 27.3 mmol) were added to the solution. The mixture was diluted with CH2Cl2 (225 mL) and cooled to 0° C. A solution of DCC (5.63 g, 27.3 mmol) in 25 mL of CH2Cl2 was added to the mixture. The mixture was stirred for 18 h while the temperature of the mixture was allowed to rise to room temperature. The reaction mixture was worked up to the same manner as described for Boc-Arg(Tos)-Ile-OFm in the preceding paragraph, except that the product obtained following the washings was purified by chromatography on silica gel, using EtOAc-hexane (1:1) as eluent, to give Boc-Arg(Tos)-Ile-Gly-OFm (13.2 g). The Boc protecting group was removed from the latter compound (13.0 g) with 1N HCl in glacial acetic acid, of Example 6 (c), to give the desired tripeptide as its HCl addition salt (12.0 g).

後処理

  1. customto rise to room temperature
  2. customobtained
  3. customwas purified by chromatography on silica gel

出典と根拠

ORDレコード
ord-21d23a910885492480be8c18b1d70a85
出典データセット
uspto-grants-1990_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04891358

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート