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Methanol → 5-Chloro-alpha-(3-tert-butoxycarbonylaminophenyl)-2-neopentylaminobenzyl alcohol

HRID 275848
ノート
印刷プレビュー

反応式

HRID 275848 の反応式
CO.[NH2:3][C:4]1[CH:25]=[CH:24][C:23]([Cl:26])=[CH:22][C:5]=1[CH:6]([OH:21])[C:7]1[CH:12]=[CH:11][CH:10]=[C:9]([NH:13][C:14]([O:16][C:17]([CH3:20])([CH3:19])[CH3:18])=[O:15])[CH:8]=1.[CH3:27][C:28]([CH3:32])([CH3:31])[CH:29]=O.C([BH3-])#N.[Na+]>C(OC(=O)C)C.C(O)(=O)C>[Cl:26][C:23]1[CH:24]=[CH:25][C:4]([NH:3][CH2:27][C:28]([CH3:32])([CH3:31])[CH3:29])=[C:5]([CH:22]=1)[CH:6]([OH:21])[C:7]1[CH:12]=[CH:11][CH:10]=[C:9]([NH:13][C:14]([O:16][C:17]([CH3:20])([CH3:19])[CH3:18])=[O:15])[CH:8]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 887MethanolHCID 12417PivalaldehydeHCID 5003444Sodium cyanoborohydrideHCID 540518662-Amino-5-chloro-alpha-(3-tert-butoxycarbonylaminophenyl)benzyl alcohol

生成物 1

HCID 538324135-Chloro-alpha-(3-tert-butoxycarbonylaminophenyl)-2-neopentylaminobenzyl alcohol収率 89.5%

試薬・触媒・溶媒 2

HCID 176
Acetic Acid
溶媒
HCID 8857Ethyl Acetate溶媒

実験手順

To a methanol (4 ml) solution of 2-amino-5-chloro-α-(3-tert-butoxycarbonylaminophenyl) benzyl alcohol (0.4 g) were added trimethyl acetaldehyde (109 mg) and acetic acid (76 mg). The mixture was stirred for 10 minutes at room temperature, to which was added sodium cyano borohydride (79 mg). The mixture was stirred for one hour at room temperature, to which was added acetic acid ethyl ester (50 ml). The mixture was washed with water and dried over anhydrous MgSO4. The solvent was then distilled off, and the residue was purified by means of a silica gel column chromatography to give the object 5-chloro-α-(3-tert-butoxycarbonylaminophenyl)-2-neopentylaminobenzyl alcohol (0.43 g) as a colorless amorphous solid product.

後処理

  1. stirringThe mixture was stirred for one hour at room temperature, to which
  2. washThe mixture was washed with water
  3. dry with materialdried over anhydrous MgSO4
  4. distillationThe solvent was then distilled off
  5. customthe residue was purified by means of a silica gel column chromatography

出典と根拠

ORDレコード
ord-c87609a865e3424f8211c7f6361e52b1
出典データセット
uspto-grants-2002_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06352982B1

反応ノート

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