1,4-Dimercapto-2,3-butanediol → 2-Morpholin-4-ylethyl (6-sulphanyl-1,3-benzothiazol-2-yl)carbamate

HRID 633486노트

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HRID 633486 반응식
[S:1]([C:4]1[CH:24]=[CH:23][C:7]2[N:8]=[C:9]([NH:11][C:12](=[O:22])[O:13][CH2:14][CH2:15][N:16]3[CH2:21][CH2:20][O:19][CH2:18][CH2:17]3)[S:10][C:6]=2[CH:5]=1)C#N.SCC(C(CS)O)O>P([O-])(O)(O)=O.[K+]>[SH:1][C:4]1[CH:24]=[CH:23][C:7]2[N:8]=[C:9]([NH:11][C:12](=[O:22])[O:13][CH2:14][CH2:15][N:16]3[CH2:21][CH2:20][O:19][CH2:18][CH2:17]3)[S:10][C:6]=2[CH:5]=1

참가 물질

4

실험 절차

The 2-morpholin-4-ylethyl (6-sulphanyl-1,3-benzothiazol-2-yl)carbamate was prepared according to the method described in Example 1b, but using 547 mg of 2-morpholin-4-ylethyl (6-thiocyanato-1,3-benzothiazol-2-yl)carbamate, 12 mg of potassium dihydrogen phosphate and 1.16 g of DL-dithiothreitol. 885 mg of 2-morpholin-4-ylethyl (6-sulphanyl-1,3-benzothiazol-2-yl)carbamate are thus obtained in the form of a white solid, the characteristics of which are as follows:

후처리

  1. customThe 2-morpholin-4-ylethyl (6-sulphanyl-1,3-benzothiazol-2-yl)carbamate was prepared

출처 및 근거

ORD 기록
ord-48aab0433a234f78a9ca483ca94cb326
출처 데이터셋
uspto-grants-2016_04
특허 번호
US09321777B2

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