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Hydrochloric Acid → HCID 19424596, 화합물

HRID 743500
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HRID 743500 반응식
[CH2:1]1[N:8]([CH2:9][CH2:10][NH+:11]([CH2:22][C:23]([O-:25])=[O:24])[CH2:12][CH2:13][N:14]2[CH2:21][C:19](=[O:20])[O:18][C:16](=[O:17])[CH2:15]2)[CH2:7][C:5](=[O:6])[O:4][C:2]1=[O:3].[NH2:26][CH2:27][CH2:28][CH2:29][CH2:30][NH2:31].Cl>CN(C=O)C.CN(C=O)C.C1CN2C(=NCCC2)C1>[C:16]([CH2:15][N:14]1[CH2:21][C:19](=[O:20])[NH:31][CH2:30][CH2:29][CH2:28][CH2:27][NH:26][C:2](=[O:3])[CH2:1][N:8]([CH2:7][C:5]([OH:6])=[O:4])[CH2:9][CH2:10][N:11]([CH2:22][C:23]([OH:25])=[O:24])[CH2:12][CH2:13]1)([OH:18])=[O:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 313Hydrochloric AcidHCID 1045PutrescineHCID 16760401Diethylenetriaminepentaacetic dianhydride

생성물 1

HCID 19424596HCID 19424596, 화합물

시약·촉매·용매 2

HCID 6228Dimethylformamide용매2회HCID 131719551HCID 131719551, 화합물용매

실험 절차

A 1 L three-neck flask was charged with 340 mL of dry DMF. Two syringes were charged separately with solutions of diethylenetriaminepentaacetic acid dianhydride (3.00 g, 8.40 mmol) in 100 mL of DMF and 1,4-diaminobutane (0.740 g, 8.40 mmol) in DMF/DBN, (96 mL/4 mL). The solutions were added simultaneously at ambient temperature to the flask at a rate of 30 mL/hour. After the addition was complete, the reaction mixture was allowed to stir overnight, stripped to dryness, and 1N HCl added to adjust the pH to 10.4. The solution was applied to AG1-X8 (100-200 mesh, OAc-) resin and eluted with 0.5N acetic acid to yield 0.52 g (13.6%) as a white solid, after removal of acetic acid and lyophilization.

후처리

  1. additionThe solutions were added simultaneously at ambient temperature to the flask at a rate of 30 mL/hour
  2. additionAfter the addition
  3. additionadded
  4. washeluted with 0.5N acetic acid
  5. customto yield 0.52 g (13.6%) as a white solid
  6. customafter removal of acetic acid and lyophilization

출처 및 근거

ORD 기록
ord-1dcdd200f8024a8398612ef6a82c7878
출처 데이터셋
uspto-grants-1996_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05556968

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