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Cyanamide → HCID 178474458, 화합물

HRID 1246442
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HRID 1246442 반응식
Cl.[C:2]([NH:5][C:6]1[S:7][CH:8]=[C:9]([C:11]([NH:13][C:14]2[CH:19]=[CH:18][C:17]([NH2:20])=[CH:16][CH:15]=2)=[O:12])[N:10]=1)(=[O:4])[CH3:3].[N:21]#[C:22][NH2:23]>COCCO>[C:2]([NH:5][C:6]1[S:7][CH:8]=[C:9]([C:11]([NH:13][C:14]2[CH:19]=[CH:18][C:17]([NH:20][C:22]([NH2:23])=[NH:21])=[CH:16][CH:15]=2)=[O:12])[N:10]=1)(=[O:4])[CH3:3]
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참가 물질

4

반응물 2

HCID 9864CyanamideHCID 219152912-(acetylamino)-N-(4-aminophenyl)-1,3-thiazole-4-carboxamide hydrochloride

생성물 1

HCID 178474458HCID 178474458, 화합물수율 63.2%

시약·촉매·용매 1

HCID 80192-Methoxyethanol용매

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온도
100 °C

실험 절차

A mixture of 2-(acetylamino)-N-(4-aminophenyl)-1,3-thiazole-4-carboxamide hydrochloride (70 mg), cyanamide (11 mg) and 2-methoxyethanol (2 ml) was stirred at 100° C. for 72 hours. The reaction mixture was concentrated in vacuo. To the residue was added ethyl acetate (5 ml) and saturated aqueous sodium hydrogen bicarbonate (5 ml). The precipitated solid was filtered and washed with ethyl acetate and water to give 2-(acetylamino)-N-(4-{[amino(imino)methyl]amino}phenyl)-1,3-thiazole-4-carboxamide (45 mg).

후처리

  1. concentrationThe reaction mixture was concentrated in vacuo
  2. additionTo the residue was added ethyl acetate (5 ml) and saturated aqueous sodium hydrogen bicarbonate (5 ml)
  3. filtrationThe precipitated solid was filtered
  4. washwashed with ethyl acetate and water

출처 및 근거

ORD 기록
ord-d3140f1d220e4021b7bc278a8c2e77da
출처 데이터셋
uspto-grants-2006_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07125901B2

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