(R)-2-(3-Chlorophenyl)-2-hydroxyacetic acid → N-[(2S)-7-hydroxy-1,2,3,4-tetrahydronaphth-2-yl]-(S)-3-chloromandelamide
반응식
[Cl:1]C1C=C(C=CC=1)[C@H](O)C(O)=O.[Cl:13][C:14]1[CH:15]=[C:16]([CH:22]=[CH:23][CH:24]=1)[C@@H:17]([OH:21])[C:18]([OH:20])=O.Cl.[NH2:26][C@H:27]1[CH2:36][CH2:35][C:34]2[C:29](=[CH:30][C:31]([OH:37])=[CH:32][CH:33]=2)[CH2:28]1>>[ClH:1].[NH2:26][C@@H:27]1[CH2:36][CH2:35][C:34]2[C:29](=[CH:30][C:31]([OH:37])=[CH:32][CH:33]=2)[CH2:28]1.[OH:37][C:31]1[CH:30]=[C:29]2[C:34]([CH2:35][CH2:36][C@H:27]([NH:26][C:18](=[O:20])[C@H:17]([C:16]3[CH:22]=[CH:23][CH:24]=[C:14]([Cl:13])[CH:15]=3)[OH:21])[CH2:28]2)=[CH:33][CH:32]=1참가 물질
5
반응물 3
생성물 2
실험 절차
By following the procedure described in PREPARATION IX and substituting the (S)-3-chloromandelic acid for the (R)-3-chloromandelic acid and the (S)-2-amino-7-hydroxytetralin hydrochloride, PREPARATION IV, for the (R)-2-amino-7-hydroxytetralin hydrochloride, the N-[(2S)-7-hydroxy-1,2,3,4-tetrahydronaphth-2-yl]-(S)-3-chloromandelamide, SR 58574, is obtained; m.p. 145°-146° C.; /alpha/=-34.2° (methanol, c=1%).
출처 및 근거
- ORD 기록
- ord-7cb7fbc20ea9462bbf6db959968ae017
- 출처 데이터셋
- uspto-grants-1994_09
- 특허 번호
- US05347037
반응 노트
불러오는 중…