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Dimethylformamide → N-2-adamantyl-4-[2-(ethylsulfonyl)ethyl]bicyclo[2.2.2]octane-1-carboxamide

HRID 605509
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반응식

HRID 605509 반응식
[CH2:1]([S:3]([CH2:6][CH2:7][C:8]12[CH2:15][CH2:14][C:11]([C:16]([OH:18])=O)([CH2:12][CH2:13]1)[CH2:10][CH2:9]2)(=[O:5])=[O:4])[CH3:2].[C:19](Cl)(=O)[C:20](Cl)=O.C[N:26]([CH:28]=O)C>C(Cl)Cl>[CH:20]12[CH2:19][CH:10]3[CH2:9][CH:8]([CH2:13][CH:12]([CH2:11]3)[CH:28]1[NH:26][C:16]([C:11]13[CH2:10][CH2:9][C:8]([CH2:7][CH2:6][S:3]([CH2:1][CH3:2])(=[O:5])=[O:4])([CH2:15][CH2:14]1)[CH2:13][CH2:12]3)=[O:18])[CH2:7]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6228DimethylformamideHCID 65578Oxalyl chlorideHCID 225917104-[2-(Ethylsulfonyl)ethyl]bicyclo[2.2.2]octane-1-carboxylic acid

생성물 1

HCID 11502385N-2-adamantyl-4-[2-(ethylsulfonyl)ethyl]bicyclo[2.2.2]octane-1-carboxamide

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

Carboxylic acid 1-4 (810 mg, 3 mmol) was dissolved in methylene chloride (5 ml) and treated with oxalyl chloride (4 eq.) and 0.050 ml of DMF. The reaction was stirred at room temperature for 45 min, then the solvent was removed under reduced pressure to give a quantitative crude yield of 4-[2-(ethylsulfonyl)ethyl]bicyclo[2.2.2]octane-1-carboxyl chloride (1-5).

후처리

  1. customthe solvent was removed under reduced pressure

출처 및 근거

ORD 기록
ord-07b8d38533af4560a9c26f88f853ad52
출처 데이터셋
uspto-grants-2011_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07915252B2

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