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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 13596127, 화합물 → HCID 178521988, 화합물

HRID 325717
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HRID 325717 반응식
C([N:8]1[C:12]([C:13]([NH:15][C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=2[O:22]CC2C=CC=CC=2)=[O:14])=[N:11][N:10]=[N:9]1)C1C=CC=CC=1>C(O)(=O)C.[Pd]>[OH:22][C:17]1[CH:18]=[CH:19][CH:20]=[CH:21][C:16]=1[NH:15][C:13]([C:12]1[NH:11][N:10]=[N:9][N:8]=1)=[O:14]
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참가 물질

4

반응물 1

HCID 13596127HCID 13596127, 화합물

생성물 1

HCID 178521988HCID 178521988, 화합물수율 42.3%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 176Acetic Acid용매

실험 절차

A solution of 1-benzyl-2'-benzyloxy-1H-tetrazole-5-carboxanilide (2.0 g) in glacial acetic acid (100 ml) was hydrogenated at 53° C. and 4.1 kg/cm2 for 18.5 hours, using a catalyst of palladium on charcoal (5% w/w). The mixture was filtered and the filtrate was evaporated at 40° C. in vacuo. The resulting solid was dissolved in a minimum volume of aqueous ammonia solution (2 N). The solution was filtered and then acidified with dilute hydrochloric acid (2 N). The resulting solid was filtered off, dried and recrystallised from aqueous dimethylformamide to give 2'-hydroxytetrazole-5-carboxanilide (0.45 g), m.p. 220°-223° C.

후처리

  1. customwas hydrogenated at 53° C.
  2. filtrationThe mixture was filtered
  3. customthe filtrate was evaporated at 40° C. in vacuo
  4. dissolutionThe resulting solid was dissolved in a minimum volume of aqueous ammonia solution (2 N)
  5. filtrationThe solution was filtered
  6. filtrationThe resulting solid was filtered off
  7. customdried
  8. customrecrystallised from aqueous dimethylformamide

출처 및 근거

ORD 기록
ord-2638b32a378041b78a0147fd7a8656a3
출처 데이터셋
uspto-grants-1984_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04442115

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