2-(Diisopropylamino)ethanethiol hydrochloride → HCID 66834810, compound

HRID 2275124Notes

Reaction equation

HRID 2275124 reaction equation
[C:1]([C:3]1[CH:15]=[C:14]2[C:6]([C:7]3[C:8](=[O:30])[C:9]4[CH:21]=[CH:20][C:19](OS(C(F)(F)F)(=O)=O)=[CH:18][C:10]=4[C:11]([CH3:17])([CH3:16])[C:12]=3[NH:13]2)=[CH:5][CH:4]=1)#[N:2].Cl.[CH:32]([N:35]([CH:39]([CH3:41])[CH3:40])[CH2:36][CH2:37][SH:38])([CH3:34])[CH3:33]>>[CH:32]([N:35]([CH:39]([CH3:41])[CH3:40])[CH2:36][CH2:37][S:38][C:19]1[CH:20]=[CH:21][C:9]2[C:8](=[O:30])[C:7]3[C:6]4[C:14](=[CH:15][C:3]([C:1]#[N:2])=[CH:4][CH:5]=4)[NH:13][C:12]=3[C:11]([CH3:16])([CH3:17])[C:10]=2[CH:18]=1)([CH3:34])[CH3:33]

Participants

3

Reactant 2

HCID 30848292-(Diisopropylamino)ethanethiol hydrochlorideHCID 86663817Trifluoro-methanesulfonic acid 3-cyano-6,6-dimethyl-11-oxo-6,11-dihydro-5H-benzo[b]carbazol-8-yl ester

Product 1

HCID 66834810HCID 66834810, compound

Procedure

Under the same conditions as the method for synthesizing Compound B2-17, the title compound was prepared from Compound B1 and 2-diisopropylaminoethanethiol hydrochloric acid salt.

Sources & evidence

ORD record
ord-c032572243e142bd94497f901f751ba0
Source dataset
uspto-grants-2015_09
Patent number
US09126931B2

Reaction notes

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