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Benzaldehyde → HCID 20284821, 화합물

HRID 127510
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HRID 127510 반응식
[NH2:1][CH2:2][CH:3]1[C:15]2[C:14]3[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=3)[NH:8][C:7]=2[S:6][CH2:5][CH2:4]1.[CH:16](=O)[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1.Cl>CO.C([BH3-])#N.[Na+]>[CH2:16]([NH:1][CH2:2][CH:3]1[C:15]2[C:7](=[N:8][C:9]3[C:14]=2[CH2:13][CH:12]=[CH:11][CH:10]=3)[S:6][CH2:5][CH2:4]1)[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 240BenzaldehydeHCID 313Hydrochloric AcidHCID 30560881-(2,3,4,9-Tetrahydrothiopyrano[2,3-b]indol-4-yl)methanamine

생성물 1

HCID 20284821HCID 20284821, 화합물수율 99.1%

시약·촉매·용매 2

HCID 887Methanol용매3회HCID 5003444Sodium cyanoborohydride
용매

실험 절차

To a solution of 4-aminomethyl-2,3,4,9-tetrahydrothiopyrano[2,3-b]indole (150 mg) in methanol (5 ml) are added a solution of benzaldehyde (76 mg) in methanol (1.5 ml) and sodium cyanoborohydride (132 mg). The mixture is adjusted to pH 7 with a solution of hydrochloride in methanol, stirred at room temperature for 1 hour and evaporated to remove the solvent. The residue is dissolved in ether, washed with a 10% aqueous solution of sodium hydroxide and a saline solution, dried and evaporated to give the title compound (210 mg).

후처리

  1. customevaporated
  2. customto remove the solvent
  3. dissolutionThe residue is dissolved in ether
  4. washwashed with a 10% aqueous solution of sodium hydroxide
  5. customa saline solution, dried
  6. customevaporated

출처 및 근거

ORD 기록
ord-84dee13c01884284825e175ee3d51cf3
출처 데이터셋
uspto-grants-1981_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04256640

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