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Leucyl-glycine-pentachlorophenyl ester.hydrochloride → 4-Methylmorpholine

HRID 1248746
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반응식

HRID 1248746 반응식
Cl.[Cl:2][C:3]1[C:8]([O:9][C:10](=[O:21])[CH2:11][NH:12][C:13](=[O:20])[C@H:14]([CH2:16][CH:17]([CH3:19])[CH3:18])[NH2:15])=[C:7]([Cl:22])[C:6]([Cl:23])=[C:5]([Cl:24])[C:4]=1[Cl:25]>CS(C)=O>[ClH:2].[Cl:2][C:3]1[C:8]([O:9][C:10](=[O:21])[CH2:11][NH:12][C:13](=[O:20])[C@H:14]([CH2:16][CH:17]([CH3:18])[CH3:19])[NH2:15])=[C:7]([Cl:22])[C:6]([Cl:23])=[C:5]([Cl:24])[C:4]=1[Cl:25].[CH3:13][N:12]1[CH2:11][CH2:10][O:9][CH2:8][CH2:3]1
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참가 물질

4

반응물 1

HCID 18598480Leucyl-glycine-pentachlorophenyl ester.hydrochloride

생성물 2

HCID 79724-Methylmorpholine수율 399.4%HCID 18598480Leucyl-glycine-pentachlorophenyl ester.hydrochloride

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매

실험 절차

In 1.5 ml of DMSO was dissolved 1.0 g of the leucyl-glycine-pentachlorophenyl ester.hydrochloride obtained in above (1), and 0.427 g of N-methylmorpholine was added. The resulting mixture was immediately placed in a thermostat at 40° C. After 2 hours, 5 hours or 12 hours, 0.30 g, 0.60 g or 0.60 g, respectively, of phosphorus pentoxide was added to the polymerization system (Run Nos. 1 to 3). When the reaction was carried out at 40° C. for 6 days in total from the addition of the tertiary amine, the whole reaction mixture solidified to become gelatinous.

출처 및 근거

ORD 기록
ord-221ec669038749019cd9f8b2c9a5300f
출처 데이터셋
uspto-grants-1985_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04525576

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