L-(+)-Cysteine → HCID 136047812, compound

HRID 63221Notes

Reaction equation

HRID 63221 reaction equation
C1(C2SC=[C:10]([C:12]([C:14]3[CH:19]=[C:18](OC)[C:17](OC)=[C:16](OC)[CH:15]=3)=O)[N:11]=2)C=CC=CC=1.[NH:26]1[C:34]2[C:29](=[CH:30][CH:31]=[CH:32][CH:33]=2)[CH:28]=[C:27]1[C:35]1[S:36][CH2:37][CH:38]([C:40]([OH:42])=O)[N:39]=1.N[C@H](C(O)=O)CS>>[NH:26]1[C:34]2[C:29](=[CH:30][CH:31]=[CH:32][CH:33]=2)[CH:28]=[C:27]1[C:35]1[S:36][CH:37]=[C:38]([C:40]([C:10]2[NH:11][C:19]3[C:14]([CH:12]=2)=[CH:15][CH:16]=[CH:17][CH:18]=3)=[O:42])[N:39]=1

Participants

4

Reactant 3

HCID 5862L-(+)-CysteineHCID 252274304-(3,4,5-Trimethoxybenzoyl)-2-phenylthiazoleHCID 57516834HCID 57516834, compound

Product 1

HCID 136047812HCID 136047812, compound

Procedure

(2-(1H-Indol-2-yl)thiazol-4-yl)(1H-indol-2-yl)methanone (8) was prepared using the similar method as used of compound 1h from 2-(1H-indol-2-yl)-4,5-dihydrothiazole-4-carboxylic acid and cysteine. 1H NMR (500 MHz, CDCl3) δ 9.39 (s, 1H), 8.54 (s, 1H), 8.46 (s, 1H), 8.06 (s, 1H), 8.03 (dd, 1H), 7.66 (d, 1H), 7.51 (d, 1H), 7.41 (d, 1H), 7.33 (t, 1H), 7.29 (d, 1H), 7.15 (t, 1H), 7.09 (d, 1H), 6.72 (s, 1H). MS (ESI) m/z 366.1 (M+Na)+, 341.9 (M−H)−.

Sources & evidence

ORD record
ord-905e9c9e0c914d4eaf146d4e6412c6ce
Source dataset
uspto-grants-2016_09
Patent number
US09447049B2

Reaction notes

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