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Hydrogen Sulfide → 2-Phenyl-4-amino-5-thiocarbamoylthiazole

HRID 262035
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HRID 262035 반응식
[C:1]1([C:7]2[S:8][C:9]([C:13]#[N:14])=[C:10]([NH2:12])[N:11]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.CN(C)C=O.[SH2:20]>C(N(CC)CC)C>[C:1]1([C:7]2[S:8][C:9]([C:13](=[S:20])[NH2:14])=[C:10]([NH2:12])[N:11]=2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1
참가 물질실험 절차출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 402Hydrogen SulfideHCID 6228DimethylformamideHCID 125263524-Amino-2-phenyl-1,3-thiazole-5-carbonitrile

생성물 1

HCID 125263552-Phenyl-4-amino-5-thiocarbamoylthiazole수율 89%

시약·촉매·용매 1

HCID 8471Triethylamine용매

실험 절차

75 parts of 2-phenyl-4-amino-5-cyanothiazole in 300 parts of dimethylformamide and 15 parts of triethylamine are reacted with 13 parts of hydrogen sulfide as described in Example 1(a). 77 parts of 2-phenyl-4-amino-5-thiocarbamoylthiazole (89% of theory) of melting point 164°-167° C. are obtained.

출처 및 근거

ORD 기록
ord-d00c3903127941638ec2242bf6843463
출처 데이터셋
uspto-grants-1979_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04153607

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