Benzyl Bromide → 3-Benzylamino-4-isopropylamino-5-sulphamyl-benzoic acid

HRID 1287794노트

반응식

HRID 1287794 반응식
[NH2:1][C:2]1[CH:3]=[C:4]([CH:8]=[C:9]([S:15](=[O:18])(=[O:17])[NH2:16])[C:10]=1[NH:11][CH:12]([CH3:14])[CH3:13])[C:5]([OH:7])=[O:6].[CH2:19](Br)[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1>C(O)C>[CH2:19]([NH:1][C:2]1[CH:3]=[C:4]([CH:8]=[C:9]([S:15](=[O:18])(=[O:17])[NH2:16])[C:10]=1[NH:11][CH:12]([CH3:13])[CH3:14])[C:5]([OH:7])=[O:6])[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1

참가 물질

4

반응물 2

HCID 7498Benzyl BromideHCID 215059903-Amino-4-isopropylamino-5-sulphamyl-benzoic acid

생성물 1

HCID 215060283-Benzylamino-4-isopropylamino-5-sulphamyl-benzoic acid

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A mixture of 3-amino-4-isopropylamino-5-sulphamyl-benzoic acid (2.62 g), benzyl bromide (4.28 g), and anhydrous ethanol (25 ml) was refluxed for 24 hours. The reaction mixture was evaporated in vacuo. 1N sodium hydroxide (30 ml) was added, and the mixture was heated on a steam bath for 1 hour. After cooling and extracting with diethyl ether, the aqueous layer was adjusted to a pH of 3 by addition of a 4N hydrochloric acid. The precipitated 3-benzylamino-4-isopropylamino-5-sulphamyl-benzoic acid was collected by suction and recrystalized from aqueous ethanol. The melting point was 233°-234° C.

후처리

  1. temperaturewas refluxed for 24 hours
  2. customThe reaction mixture was evaporated in vacuo
  3. addition1N sodium hydroxide (30 ml) was added
  4. temperaturethe mixture was heated on a steam bath for 1 hour
  5. temperatureAfter cooling
  6. extractionextracting with diethyl ether
  7. additionthe aqueous layer was adjusted to a pH of 3 by addition of a 4N hydrochloric acid
  8. customThe precipitated 3-benzylamino-4-isopropylamino-5-sulphamyl-benzoic acid was collected by suction
  9. customrecrystalized from aqueous ethanol

출처 및 근거

ORD 기록
ord-995f39cef23e4df9a0070e07fc1abe91
출처 데이터셋
uspto-grants-1976_10
특허 번호
US03985777

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