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Hydrochloric Acid → HCID 178508892, 화합물

HRID 1957571
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HRID 1957571 반응식
C([O:3][C:4](=[O:35])[CH2:5][NH:6][S:7]([C:10]1[S:11][C:12]([CH2:15][CH2:16][CH:17]2[CH2:34][NH:33][C:20]3[N:21]=[C:22]([NH:26]C(=O)C(C)(C)C)[N:23]=[C:24]([OH:25])[C:19]=3[CH2:18]2)=[CH:13][CH:14]=1)(=[O:9])=[O:8])C.Cl>[OH-].[Na+]>[NH2:26][C:22]1[N:23]=[C:24]([OH:25])[C:19]2[CH2:18][CH:17]([CH2:16][CH2:15][C:12]3[S:11][C:10]([S:7]([NH:6][CH2:5][C:4]([OH:35])=[O:3])(=[O:8])=[O:9])=[CH:14][CH:13]=3)[CH2:34][NH:33][C:20]=2[N:21]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 178472926HCID 178472926, 화합물

생성물 1

HCID 178508892HCID 178508892, 화합물수율 109.2%

시약·촉매·용매 1

HCID 14798Sodium Hydroxide용매

실험 절차

A solution of 33 mg (0.062 mmol) of N-{5-[2-(2-pivaloylamino-4-hydroxy-5,6,7,8-tetrahydropyrido[2,3-d]pyrimidin-6-yl)-ethyl]thien-2-ylsulfonyl}glycine ethyl ester in 3.0 mL of 1.0N sodium hydroxide was stirred at room temperature for 24 hours. The reaction mixture was then acidified with 1.0N hydrochloric acid and the white precipitate was collected by filtration to give 28 mg of N-{5-[2-(2-amino-4-hydroxy-5,6,7,8-tetrahydropyrido[2,3-d]pyrimidin-6-yl)-ethyl]thien-2-ylsulfonyl}glycine.

후처리

  1. filtrationthe white precipitate was collected by filtration

출처 및 근거

ORD 기록
ord-a94fbbaa178f4f23b6297561dfebce45
출처 데이터셋
uspto-grants-1998_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05786358

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