Acetic Acid → 2-(5-Bromo-7-fluoro-1,2,3,4-tetrahydrocyclopenta[b]indol-3-yl)acetic acid
反応式
[Br:1][C:2]1[C:10]2[N:9](CC3C=CC(Cl)=CC=3)[C:8]3[CH:19]([CH2:22][C:23]([OH:25])=[O:24])[CH2:20][CH2:21][C:7]=3[C:6]=2[CH:5]=[C:4]([F:26])[CH:3]=1.N1C=CC=CC=1.BrBr.C(O)(=O)C>ClCCl.[Zn]>[Br:1][C:2]1[C:10]2[NH:9][C:8]3[CH:19]([CH2:22][C:23]([OH:25])=[O:24])[CH2:20][CH2:21][C:7]=3[C:6]=2[CH:5]=[C:4]([F:26])[CH:3]=1参加物
反応物 4
生成物 1
試薬・触媒・溶媒 2
実験手順
A slurry of the DCHA salt from Step 1 above in dichloromethane (0.241 M solution) was cooled to −20 to −15° C. Pyridine (2 eq.) was added in one shot and to the slurry was added dropwise bromine (2.5 eq.) over 30 to 45 minutes maintaining the temperature between −20° C. and −15° C. (At about ⅓ addition of bromine, the reaction mixture was thick and an efficient stirring was needed. Eventually, at about ½ addition of bromine, the mixture became “loose” again.) After completion of the addition, the reaction mixture was aged for one additional hour at −15° C. Acetic acid (3.04 eq.) was then added over 5 minutes and zinc dust (3.04 eq.) was added portion wise. (A portion of zinc was added at −15° C. and the mixture was aged for about 5 minutes to ensure that the exotherm was going (about −15° C. to −10° C.)). This operation was repeated with about 5 shots of zinc over about 30 min. When no more exotherm was observed, the remaining zinc was added faster. The whole operation takes around 30 to 45 minutes.
後処理
- temperaturemaintaining the temperature between −20° C. and −15° C. (
- addition) After completion of the addition
- customwas aged for one additional hour at −15° C
- custom(about −15° C. to −10° C.)
- waitThe whole operation takes around 30 to 45 minutes
出典と根拠
- ORDレコード
- ord-9b3c1c50f96447a1ae23a094e1784b2e
- 出典データセット
- uspto-grants-2008_01
- 特許番号
- US07317036B2
反応ノート
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