(1R,3R)-3-Aminocyclohexane-1-carboxylic acid 2,2,2-trifluoroacetic acid salt → ((1R,3R)-3-Aminocyclohexyl)methanol
反応式
FC(F)(F)C(O)=O.[NH2:8][C@@H:9]1[CH2:14][CH2:13][CH2:12][C@@H:11]([C:15](O)=[O:16])[CH2:10]1.Cl.N[C@H]1CC[C@H](C(O)=O)CC1>>[NH2:8][C@@H:9]1[CH2:14][CH2:13][CH2:12][C@@H:11]([CH2:15][OH:16])[CH2:10]1参加物
3
実験手順
((1R,3R)-3-Aminocyclohexyl)methanol was synthesized as a white powder (213 mg, 75%) using a procedure analogous to that described in Step 1 of Example 179, substituting (1R,3R)-3-aminocyclohexanecarboxylic acid trifluoroacetate from the previous step for trans-4-aminocyclohexanecarboxylic acid hydrochloride used in Example 179.
出典と根拠
- ORDレコード
- ord-9071586c0a234dc1aca2ff05541e819d
- 出典データセット
- uspto-grants-2015_02
- 特許番号
- US08952058B2
反応ノート
読み込み中…