4,5,6,7-Tetrahydro-benzothiazole-2,6-diamine dihydrobromide → HCID 10051154, compound

HRID 2113050Notes

Reaction equation

HRID 2113050 reaction equation
[CH2:1]([S:8]([NH:11][C:12]1[C:13](=[O:23])[N:14]([CH2:19][C:20](O)=[O:21])[C:15]([CH3:18])=[CH:16][CH:17]=1)(=[O:10])=[O:9])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Br.Br.[S:26]1[C:30]2[CH2:31][CH:32]([NH2:35])[CH2:33][CH2:34][C:29]=2[N:28]=[C:27]1[NH2:36]>>[NH2:36][C:27]1[S:26][C:30]2[CH2:31][CH:32]([NH:35][C:20](=[O:21])[CH2:19][N:14]3[C:15]([CH3:18])=[CH:16][CH:17]=[C:12]([NH:11][S:8]([CH2:1][C:2]4[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=4)(=[O:10])=[O:9])[C:13]3=[O:23])[CH2:33][CH2:34][C:29]=2[N:28]=1

Participants

3

Procedure

The title compound was prepared from 2-[3-[(benzylsulfonyl)amino]-6 -methyl-2-oxo-1(2H)-pyridinyl]acetic acid and 4,5,6,7-tetrahydro-1,3-benzothiazol-2,6-diamine dihydrobromide using the procedure of EXAMPLE 1 (STEP 6), and was obtained as an off-white solid compound.

Workup

  1. customwas obtained as an off-white solid compound

Sources & evidence

ORD record
ord-4bdbd7b8ea94406281d576b95c1bacba
Source dataset
uspto-grants-2009_04
Patent number
US07524871B2

Reaction notes

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