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Hydrochloric Acid → 3-(methylamino)-5-(1H-pyrazol-4-yl)thiophene-2-carboxamide dihydrochloride

HRID 2364023
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인쇄 미리보기

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HRID 2364023 반응식
[CH3:1][N:2]1[C:7]2[CH:8]=[C:9]([C:11]3[CH:12]=[N:13][NH:14][CH:15]=3)[S:10][C:6]=2[C:5](=[O:16])[NH:4]C1(C)C.[ClH:19]>CO>[ClH:19].[ClH:19].[CH3:1][NH:2][C:7]1[CH:8]=[C:9]([C:11]2[CH:15]=[N:14][NH:13][CH:12]=2)[S:10][C:6]=1[C:5]([NH2:4])=[O:16]
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참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 667433581,2,2-trimethyl-6-(1H-pyrazol-4-yl)-2,3-dihydrothieno[3,2-d]pyrimidin-4(1H)-one

생성물 1

HCID 667434043-(methylamino)-5-(1H-pyrazol-4-yl)thiophene-2-carboxamide dihydrochloride수율 99%

시약·촉매·용매 1

HCID 887Methanol용매

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온도
50 °C

실험 절차

A mixture of 1,2,2-trimethyl-6-(1H-pyrazol-4-yl)-2,3-dihydrothieno[3,2-d]pyrimidin-4(1H)-one (262 mg, 1.00 mmol), 1 M HCl (5 mL) and MeOH (5 mL) was stirred at 50° C. for 1 h. The mixture was concentrated under reduced pressure to afford the title compound (292 mg, 99%) as a pale yellow solid. This material was used for the next reaction without further purification.

후처리

  1. concentrationThe mixture was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-0227be9669794d60aa2582eea9159518
출처 데이터셋
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08691828B2

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