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HCID 178522682, 화합물 → HCID 178522681, 화합물

HRID 614808
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HRID 614808 반응식
C([O:8][C:9]1[CH:22]=[CH:21][C:20]([Cl:23])=[CH:19][C:10]=1[C:11]([NH:13][C:14]1[NH:18][N:17]=[N:16][N:15]=1)=[O:12])C1C=CC=CC=1>CN1CCCC1=O.[Pd]>[Cl:23][C:20]1[CH:21]=[CH:22][C:9]([OH:8])=[C:10]([CH:19]=1)[C:11]([NH:13][C:14]1[NH:18][N:17]=[N:16][N:15]=1)=[O:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 178522682HCID 178522682, 화합물

생성물 1

HCID 178522681HCID 178522681, 화합물수율 76.5%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 13387N-methyl-2-pyrrolidone용매

실험 절차

A solution of 2-benzyloxy-5-chloro-N-(tetrazol-5-yl)benzamide (2.7 g) in N-methylpyrrolid-2-one (50 ml) was hydrogenated at 25° C. and 5 kg/cm2 pressure using a 5% w/w palladium on charcoal catalyst. The reaction mixture was filtered and then evaporated under vacuum and the resulting solid was triturated with water and then dried. This solid was boiled with ethanol (50 ml) for 10 minutes and the undissolved material was filtered off and washed with ethanol and with diethyl ether to give 5-chloro-2-hydroxy-N-(tetrazol-5-yl)benzamide (1.5 g), m.p. 266°-269° C. (with decomposition).

후처리

  1. customwas hydrogenated at 25° C.
  2. filtrationThe reaction mixture was filtered
  3. customevaporated under vacuum
  4. customthe resulting solid was triturated with water
  5. customdried
  6. filtrationthe undissolved material was filtered off
  7. washwashed with ethanol and with diethyl ether

출처 및 근거

ORD 기록
ord-ee5b6f97b6f247e5af603fa1c21de19b
출처 데이터셋
uspto-grants-1979_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04146631

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