Boron tribromide → HCID 53847727、化合物

HRID 1684088ノート

反応式

HRID 1684088 の反応式
B(Br)(Br)Br.Cl.[F:6][C:7]1[CH:8]=[CH:9][C:10]([O:26]C)=[C:11]2[C:16]=1[O:15][CH2:14][C@H:13]([N:17]([CH:21]([CH2:24][CH3:25])[CH2:22][CH3:23])[CH2:18][CH2:19][CH3:20])[CH2:12]2>C(Cl)Cl>[F:6][C:7]1[CH:8]=[CH:9][C:10]([OH:26])=[C:11]2[C:16]=1[O:15][CH2:14][C@H:13]([N:17]([CH:21]([CH2:22][CH3:23])[CH2:24][CH3:25])[CH2:18][CH2:19][CH3:20])[CH2:12]2

参加物

4

反応物 2

HCID 25134Boron tribromideHCID 67703428HCID 67703428、化合物

生成物 1

HCID 53847727HCID 53847727、化合物収率 98.4%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

反応条件

温度
0 °C

実験手順

Demethylation was done by addition of BBr3 (2.6 ml, 27.5 mmol) in 10 ml dry CH2Cl2 during 20 min., to a stirred, cooled solution (-70° C.) of (R)-8-fluoro-5-methoxy-3-(N-3-pentyl-N-n-propylamino)chroman hydrochloride (4.44 g, 12.8 mmol) in 100 ml dry CH2Cl2 under N2 atmosphere and dry conditions. The solution was stirred for 1 hour at -70° C., 1 hour at 0° C. and 1 hour at room temp. and was thereafter poured into 80 ml saturated. NaHCO3 aq. under vigirous stirring. After 0.5 hour the layers where separated and the aqueous phase was extracted with 2×15 ml CH2Cl2. The combined organic layers where dried (Na2SO4) and evaporated. The crude product was purified by flash chromatography on silica with a gradient of petroleumether-petroleumether: EtOAc, 4:1 to give 3.72 g of (R)-8-fluoro-5-hydroxy-3-(N-3-pentyl-N-n-propylamino)chroman (NAG 134) as an yellow-brown oil. [α]D22 ×85° (c 1.02 in MeOH).

後処理

  1. customdry conditions
  2. additionwas thereafter poured into 80 ml saturated
  3. customAfter 0.5 hour the layers where separated
  4. extractionthe aqueous phase was extracted with 2×15 ml CH2Cl2
  5. dry with materialThe combined organic layers where dried (Na2SO4)
  6. customevaporated
  7. customThe crude product was purified by flash chromatography on silica with a gradient of petroleumether-petroleumether

出典と根拠

ORDレコード
ord-b6c4bac702f048e2aac7af86eedb2cfb
出典データセット
uspto-grants-1997_06
特許番号
US05639772

反応ノート

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