반응식
[CH2:1]1[C:13]2[NH:12][C:11]3[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=3)[C:5]=2[CH2:4][C@H:3]([C:14]([OH:16])=[O:15])[NH:2]1.[OH-].[K+].[CH2:19](Cl)[C:20]1[O:24][CH:23]=[CH:22][CH:21]=1.C(O)C1OC=CC=1.S(Cl)(Cl)=O.[C:37](=[S:39])=[S:38]>N1C=CC=CC=1.C(O)C>[CH2:19]([S:39][C:37]([N:2]1[C@@H:3]([C:14]([OH:16])=[O:15])[CH2:4][C:5]2[C:6]3[C:11](=[CH:10][CH:9]=[CH:8][CH:7]=3)[NH:12][C:13]=2[CH2:1]1)=[S:38])[C:20]1[O:24][CH:23]=[CH:22][CH:21]=1참가 물질
9
실험 절차
In the same manner as descsribed in Example 32, (3R)-1,2,3,4-tetrahydro-β-carboline-3-carboxylic acid (8.65 g), KOH (4.67 g), carbon disulfide (2.43 ml), 75% ethanol (120 ml) and furfuryl chloride which is prepared from furfuryl alcohol (9.24 g), thionyl chloride (12.34 g) and pyridine (8.94 g) are reacted and treated to give the title compound (2.31 g) as pale yellow powder.
후처리
- customare reacted
- additiontreated
출처 및 근거
- ORD 기록
- ord-4d04b1f0650b4fee9de48418bb2f4bae
- 출처 데이터셋
- uspto-grants-1986_12
- 특허 번호
- US04628057
연결된 노트
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